510(k) K123462 ยท PDU Catheter For Crossing Total Occlusions
OCELOT CATHETER
| Applicant | Avinger, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Dec 7, 2012 |
| Received | Nov 9, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123462
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.