510(k) K831568 ยท HHF Remover, Intrauterine Device, Contraceptive, Hook-Type
RELIANCE TEMPO OPHTH. INSTR STAND
| Applicant | F. & F. Koenigkramer, Walker MI, US |
| Decision | Substantially Equivalent, Jun 30, 1983 |
| Received | May 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831568
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.