510(k) K831817 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PATIENT MONITOR #RM-100
| Applicant | Honeywell, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 31, 1983 |
| Received | Jun 6, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831817
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.