510(k) K982657 ยท MCW Catheter, Peripheral, Atherectomy
AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100
| Applicant | Microvena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, Nov 18, 1998 |
| Received | Jul 30, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982657
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.