510(k) K831164 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PATIENT MONITOR CM 135
| Applicant | Honeywell, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 1, 1983 |
| Received | Apr 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831164
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.