510(k) K094062 ยท DQX Wire, Guide, Catheter
PERCU-PRO GUIDEWIRE
| Applicant | Cardiosolutions, Inc., Stoughton MA, US |
| Decision | Substantially Equivalent, Sep 27, 2010 |
| Received | Dec 31, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K094062
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.