510(k) K062868 ยท DQY Catheter, Percutaneous
THE CROSSER CATHETER, MODEL CR1100 AND SYSTEM ELECTRONICS, MODEL FG1002-02
| Applicant | Flowcardia, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jan 19, 2007 |
| Received | Sep 25, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062868
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.