510(k) K131492 ยท DQY Catheter, Percutaneous
MODIFIED FLOWGATE BALLOON GUIDE CATHETER
| Applicant | Concentric Medical, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Oct 3, 2013 |
| Received | May 23, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131492
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.