510(k) K053491 ยท DQY Catheter, Percutaneous
PENUMBRA BALLOON GUIDE CATHETER, MODEL 7.5F
| Applicant | Penumbra, Inc., San Leandro CA, US |
| Decision | Substantially Equivalent, Apr 27, 2006 |
| Received | Dec 15, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053491
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.