510(k) K852039 ยท JYG Curette, Ear
FLEX-LOOP FLEXIBLE EAR CORETTE
| Applicant | Bionix Corp., Holland OH, US |
| Decision | Substantially Equivalent, Jun 11, 1985 |
| Received | May 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852039
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.