Shelf Life of Medical Devices
Detailed guidance document from FDA and regulatory agencies.
Document Details
Guidance Document
April 1, 1991
March 17, 2020
1f8de165-791b-40a8-80ef-bb23aaa44467
Related Documents
Guidance on Premarket Notification [510(k)] Submissions for Automated Endoscope Washers, Washer/Disinfectors, and Disinfectors Intended for Use in Health Care Facilities
Guidance DocumentAugust 1, 1993Center 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
Guidance on the Content and Format of Premarket Notification [510(k)] Submissions for Sharps Containers
Guidance DocumentOctober 1, 1993Center for Devices and Radiological Health
Quick Actions
Transform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Stay ahead of FDA enforcement
New KeyPedia insights, webinars, and regulatory analysis — straight to your inbox. Unsubscribe anytime.