510(k) K891334 ยท FZS Curette, Surgical, General Use
ACU-CURETTE
| Applicant | Acuderm, Inc., Ft. Lauderdale FL, US |
| Decision | Substantially Equivalent, Apr 11, 1989 |
| Received | Mar 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891334
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.