510(k) K903992 ยท HGM System, Monitoring, Perinatal
CYGNET CENTRAL
| Applicant | Cygnet Co., Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Dec 19, 1990 |
| Received | Aug 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903992
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.