510(k) K933238 ยท MCW Catheter, Peripheral, Atherectomy
ROTABLATOR, MODIFICATION
| Applicant | Heart Technology, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Aug 24, 1993 |
| Received | Jun 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933238
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.