510(k) K080583 ยท DQY Catheter, Percutaneous
MODIFIED HD GUIDE CATHETER
| Applicant | Concentric Medical, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Jul 18, 2008 |
| Received | Mar 3, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080583
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.