510(k) K842295 ยท HHF Remover, Intrauterine Device, Contraceptive, Hook-Type
INTRAUTERINE DEVICE REMOVER
| Applicant | Premier Dental Products Co., Norristown PA, US |
| Decision | Substantially Equivalent, Oct 12, 1984 |
| Received | Jun 11, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842295
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.