510(k) K894036 ยท HGM System, Monitoring, Perinatal
TOITU FETAL ACTOCARDIOGRAPH, MT-332
| Applicant | Toitu of America, Inc., Wayne PA, US |
| Decision | Substantially Equivalent, Nov 6, 1989 |
| Received | Jun 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894036
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.