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121
Guidance for submission of information on medical ultraviolet lamps pursuant to 21 CFR 1002.10 and 1002.12
Rockville, Md. : U.S. Dept. of Health, Education, and Welfare, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985“…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
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122
Medical device listing information and instructions
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984“…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
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123
Classification names for medical devices and in vitro diagnostic products
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991“…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
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124
Emerging electromagnetic medicine
New York : Springer-Verlag, 1990Call Number: Loading…
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125
Quality control guide for sunlamp products.
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984“…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
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126
Guide for the filing of annual reports for x-ray components and systems
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1985“…Center for Devices and Radiological Health (U.S.). Office of Compliance…”
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127
Import and export regulatory requirements for medical devices
Rockville, Md. : Washington, D.C. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; For sale by the Supt. of Docs., U.S. G.P.O., 1988“…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
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128
Medical device GMP guidance for FDA investigators
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administrationn, Center for Devices and Radiological Health, 1984“…Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance…”
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129
Annual report
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130
Device recalls : a study of quality problems
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1990“…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
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131
Medical devices standards activities report
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132
Guideline for the manufacture of in vitro diagnostic products.
Rockville, Md. : Division of Compliance Programs, Office of Compliance and Surveillance, Center for Devices and Radiological Health, Food and Drug Administration, 1990“…Center for Devices and Radiological Health (U.S.). Division of Compliance Programs…”
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133
The regulation of AIDS-related medical devices by Rivera, Richard J.
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1991“…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
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134
Premarket notification--510(k) : regulatory requirements for medical devices
Rockville, Md. : Washington, D.C. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; For sale by the Supt. of Docs., U.S. G.P.O., 1988“…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
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135
Medical devices standards activities report
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989“…Center for Devices and Radiological Health (U.S.). Office of Standards and Regulations…”
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136
Clarification of radiation control regulations for diagnostic x-ray equipment
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989“…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
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137
Preproduction quality assurance planning : recommendations for medical device manufacturers
Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1989“…Center for Devices and Radiological Health (U.S.). Office of Compliance and Surveillance…”
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138
Center for Devices and Radiological Health publications index
Rockville, Md. : The Center, 1988“…Center for Devices and Radiological Health (U.S.). Publications Support Branch…”
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139
Premarket approval (PMA) manual
Rockville, Md. : [Washington, D.C.] : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; [Supt. of Docs., U.S. G.P.O., distributor], 1986“…Center for Devices and Radiological Health (U.S.). Office of Device Evaluation…”
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140
Device good manufacturing practices manual
Rockville, Md. : Washington, D.C. : The Office ; For sale by the Supt. of Docs., U.S. G.P.O., 1984“…Center for Devices and Radiological Health (U.S.). Office of Training and Assistance…”
3d ed.
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