510(k) K984306 ยท MFD Cannula, Intrauterine Insemination
`THE INSEMINATOR' (PROPOSED)
| Applicant | Wallach Surgical Devices, Inc., Orange CT, US |
| Decision | Substantially Equivalent, Mar 1, 1999 |
| Received | Dec 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984306
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.