510(k) K982630 ยท MFD Cannula, Intrauterine Insemination
MEDWORKS VISUALIZATION INSEMINATION CATHETER
| Applicant | Medworks Corp., Pawtucket RI, US |
| Decision | Substantially Equivalent, Jan 14, 1999 |
| Received | Jul 28, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982630
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.