510(k) K102418 ยท DQY Catheter, Percutaneous
REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM
| Applicant | Reverse Medical Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Apr 15, 2011 |
| Received | Aug 25, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102418
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.