510(k) K924712 ยท MCW Catheter, Peripheral, Atherectomy
ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM
| Applicant | Hearing Tech, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Dec 8, 1992 |
| Received | Sep 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924712
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.