510(k) K954351 ยท HGM System, Monitoring, Perinatal
SERIES 50XM
| Applicant | Hewlett-Packard GmbH, Wuerttemberg, DE |
| Decision | Substantially Equivalent, Mar 8, 1996 |
| Received | Sep 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954351
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.