Third Party Review Guidance For Vitreous Aspiration and Cutting Device Premarket Notification (510(k))
Detailed guidance document from FDA and regulatory agencies.
Document Details
Guidance Document
January 30, 1997
Center for Devices and Radiological Health
49a8b1be-5823-4c6e-bc2c-1109bce662bd
Related Documents
Review Guidelines for Oxygen Generators and Oxygen Equipment for Emergency Use
Guidance DocumentJanuary 1, 1977
Guidance for the Content of Premarket Notifications for Conventional and Antimicrobial Foley Catheters
Guidance DocumentSeptember 11, 1994
Guidance on the Content of Premarket Notification [510(K)] Submissions for Piston Syringes
Guidance DocumentMarch 31, 1993
Quick Actions
Transform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust KeyPedia for their regulatory compliance needs.