510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
OBCClass III

Occluder, Internal Vessel, Temporary

Unknown
FDA source (opens on fda.gov)

OBC is the FDA product code for Occluder, Internal Vessel, Temporary, a class III device type. FDA's definition for this code reads: "For temporarily occluding vessels during anastomosis procedures". As of , FDA records hold no 510(k) clearances under this code and 18 recalls.

Classification record

Product code
OBC
Device name
Occluder, Internal Vessel, Temporary
FDA definition
For temporarily occluding vessels during anastomosis procedures.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
18

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code OBC.