Premarket notification, 510(k) : regulatory requirements for medical devices / prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance (HHS publication ; FDA 83-4158)
Premarket notification, 510(k) : regulatory requirements for medical devices / prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance
(HHS publication ; FDA 83-4158)
国立国会図書館請求記号
YCA-HE 20.4606:P 91
国立国会図書館書誌ID
000006518558
資料種別
図書
著者
Center for Devices and Radiological Health (U.S.) . Division of Small Manufacturers Assistance
Physical description for original version: vi, 30 p. ; 28 cm
原資料等に関する注記
原資料の出版事項: Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health, 1984