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- catalog alternative "Regulatory requirements for medical devices.".
- catalog contributor b2903801.
- catalog contributor b2903802.
- catalog coverage "United States".
- catalog created "[1990]".
- catalog date "1990".
- catalog date "[1990]".
- catalog dateCopyrighted "[1990]".
- catalog description "Includes bibliographical references.".
- catalog extent "vi, 69 p. :".
- catalog hasFormat "Premarket notification, 510(k).".
- catalog isFormatOf "Premarket notification, 510(k).".
- catalog isPartOf "HHS publication ; FDA 90-4158".
- catalog isPartOf "HHS publication ; no. (FDA) 90-4158.".
- catalog isPartOf "Medical devices".
- catalog issued "1990".
- catalog issued "[1990]".
- catalog language "eng".
- catalog publisher "Rockville, Md. : U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration, Center for Devices and Radiological Health ; Washington, D.C. : For sale by the Supt. of Docs., U.S. G.P.O.,".
- catalog relation "Premarket notification, 510(k).".
- catalog spatial "United States".
- catalog spatial "United States.".
- catalog subject "Consumer Product Safety standards United States Guideline.".
- catalog subject "Consumer Product Safety standards United States Legislation.".
- catalog subject "Equipment Safety standards United States Guideline.".
- catalog subject "Equipment Safety standards United States Legislation.".
- catalog subject "Equipment and Supplies standards".
- catalog subject "Medical instruments and apparatus Safety regulations United States.".
- catalog subject "R856 .P74 1990".
- catalog subject "W 26 P925 1990".
- catalog title "Premarket notification, 510(k) : regulatory requirements for medical devices / prepared by Division of Small Manufacturers Assistance, Office of Training and Assistance.".
- catalog title "Regulatory requirements for medical devices.".
- catalog type "Guideline.".
- catalog type "text".