Letter - Manufacturers, Distributors and Importers of Condom Products (included in Condom Packet 398) : Letter - Manufacturers, Distributors and Importers of Condom Products
Detailed guidance document from FDA and regulatory agencies.
Document Details
Guidance Document
February 23, 1994
March 17, 2020
4691242f-f73b-463c-ae81-9a1f76104905
Related Documents
Shelf Life of Medical Devices
Guidance DocumentApril 1, 1991Center for Devices and Radiological Health
Labeling - Regulatory Requirements for Medical Devices (FDA 89-4203)
Guidance DocumentSeptember 1, 1989Center for Devices and Radiological Health
Guidance on Premarket Notification [510(k)] Submissions for Surgical Gowns and Surgical Drapes
Guidance DocumentAugust 1, 1993Center for Devices and Radiological Health
Quick Actions
Transform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust KeyPedia for their regulatory compliance needs.