510(k) K820115 ยท HHF Remover, Intrauterine Device, Contraceptive, Hook-Type
EMMETT IUD THREAD RETREIVER
| Applicant | Proto-Med, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 5, 1982 |
| Received | Jan 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820115
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.