510(k) K130381 ยท QEW Peripheral Mechanical Thrombectomy With Aspiration
ANGIOJET ULTRA POWER PULSE KIT
| Applicant | Medrad, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 29, 2013 |
| Received | Feb 14, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130381
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.