510(k) K923634 ยท MFD Cannula, Intrauterine Insemination
MODIFIED F-10 CULTURE MEDIUM
| Applicant | Life-Tech Intl., Inc., Houston TX, US |
| Decision | Substantially Equivalent, Sep 7, 1993 |
| Received | Jul 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923634
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.