510(k) K130752 ยท KMI Monitor, Bed Patient
DYNASENSE SYSTEM
| Applicant | Centauri Medical, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 15, 2013 |
| Received | Mar 19, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130752
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.