510(k) K073221 ยท HGM System, Monitoring, Perinatal
CADENCE II
| Applicant | Edan Instruments, Inc., Yonkers NY, US |
| Decision | Substantially Equivalent, Dec 28, 2007 |
| Received | Nov 15, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K073221
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.