510(k) K094048 ยท DYG Catheter, Flow Directed
PERCUPRO MESSENGER BALLOON CATHETER
| Applicant | Cardiosolutions, Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Jul 14, 2011 |
| Received | Dec 31, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K094048
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.