510(k) K872354 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
SERIES 2000 BEDSIDE PATIENT MONITOR
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jul 21, 1987 |
| Received | Jun 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872354
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.