510(k) K953719 ยท MFD Cannula, Intrauterine Insemination
HUMAN TUBAL FLUID
| Applicant | Life Technologies, Inc., Grand Island NY, US |
| Decision | Substantially Equivalent, Nov 6, 1995 |
| Received | Aug 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953719
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.