510(k) K912890 ยท HGM System, Monitoring, Perinatal
MODEL SONICAID AXIS
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Jan 9, 1992 |
| Received | Jul 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912890
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.