510(k) K980061 ยท MFD Cannula, Intrauterine Insemination
EMBRYON INTRAUTERINE INSEMINATION CATHETER, EMRYON SOFT INTRAUTERINE INSEMINATION CATHETER, STYLET FOR EMBRYON INTRAUTER
| Applicant | Rocket Medical Plc, Stamford CT, US |
| Decision | Substantially Equivalent, Mar 2, 1998 |
| Received | Jan 7, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980061
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.