510(k) K945071 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PROPAQ 200 MONITOR
| Applicant | Protocol Systems, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, May 10, 1995 |
| Received | Oct 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945071
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.