510(k) K091563 ยท MMX Device, Percutaneous Retrieval
RECRUIT MICROCATHETER
| Applicant | Reverse Medical Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 30, 2009 |
| Received | May 28, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091563
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.