510(k) K051038 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
506 PATIENT MONITOR
| Applicant | Ciriticare Systems, Inc., Waukesha WI, US |
| Decision | Substantially Equivalent, Aug 12, 2005 |
| Received | Apr 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051038
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.