510(k) K901206 ยท MCW Catheter, Peripheral, Atherectomy
ROTABLATOR
| Applicant | Heart Technology, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Sep 14, 1990 |
| Received | Mar 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901206
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.