Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
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Featured books
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- GFGuidance for medical glovesCenter for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Guidance for medical gloves
no cover - MDMedical device, Federal registe...Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Medical device, Federal register documents, February 13, 1976 to October 26, 1989
no cover - PNPremarket notification, 510(k)Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Premarket notification, 510(k)
no cover - IDInvestigational device exemptio...Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Investigational device exemptions manual
no cover - RRRegulatory requirements for med...Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Regulatory requirements for medical devices
no cover - IAImport and exportCenter for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Import and export
no cover - IDInvestigational device exemptionsCenter for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Investigational device exemptions
no cover - LLabelingCenter for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Labeling
no cover - IRImport/export regulatory requir...Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Import/export regulatory requirements for medical devices
no cover - MDMedical device GMP guidance for...Center for Devices and Radiological Health (U.S.). Division of Small Manufacturers Assistance
Medical device GMP guidance for FDA investigators
no cover
Works in catalog
Quick navigation into the work-level grouping pages behind the featured books.
- Open Work
Guidance for medical gloves
- Open Work
Medical device, Federal register documents, February 13, 1976 to October 26, 1989
- Open Work
Premarket notification, 510(k)
- Open Work
Investigational device exemptions manual
- Open Work
Regulatory requirements for medical devices
- Open Work
Import and export
- Open Work
Investigational device exemptions
- Open Work
Labeling
- Open Work
Import/export regulatory requirements for medical devices
- Open Work
Medical device GMP guidance for FDA investigators