510(k) K900311 ยท DXE Catheter, Embolectomy
ARTERIAL EMBOLECTOMY CATHETER
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Jul 17, 1990 |
| Received | Jan 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900311
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.