510(k) K112262 ยท DQY Catheter, Percutaneous
REFLEX BALLON GUIDE CATHETER
| Applicant | Reverse Medical Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 2, 2011 |
| Received | Aug 8, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112262
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.