510(k) K855125 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM
| Applicant | Honeywell, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Mar 26, 1986 |
| Received | Dec 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855125
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.