510(k) K080765 ยท DQX Wire, Guide, Catheter
CROSSER LP SYSTEM
| Applicant | Flowcardia, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jun 20, 2008 |
| Received | Mar 18, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080765
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.