510(k) K951835 ยท MFD Cannula, Intrauterine Insemination
MODIFIED HUMAN TUBAL FLUID (MHTF) WITH/WITHOUT PENICILLIN G DOLIUM, WITH/WITHOUT STREPTOMYCIN SULFATE
| Applicant | Life Technologies, Inc., Grand Island NY, US |
| Decision | Substantially Equivalent, Aug 11, 1995 |
| Received | Apr 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951835
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.