510(k) K761201 ยท HGM System, Monitoring, Perinatal
ECHO-CARDIOTRACE, AUTOMATIC
| Applicant | Metrix Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 12, 1977 |
| Received | Dec 6, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K761201
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.