510(k) K910882 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PROPAQ 102EL, 104EL AND 106EL
| Applicant | Protocol Systems, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, May 8, 1991 |
| Received | Mar 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910882
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.