FDA Device Intelligence
HomeDevice types › OBC

Occluder, Internal Vessel, Temporary

FDA product code OBC · Class 3 · Unknown

2
Registered devices
8
Adverse events
18
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)
2013-06-21Genzyme Corporation, A Sanofi CompanyProduct contains particulates (fibers)

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.