510(k) K840766 ยท HTD Forceps
JANACEK TUBO-UTERINE IMPLANTATION SET
| Applicant | Cimed Intl., Inc., Kansas City MO, US |
| Decision | Substantially Equivalent, Apr 23, 1984 |
| Received | Feb 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840766
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.