510(k) K002503 ยท HGM System, Monitoring, Perinatal
FETALGARD LITE
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, Nov 9, 2000 |
| Received | Aug 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002503
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.