510(k) K002725 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MICROPAQ, MODELS 402 AND 404
| Applicant | Protocol Systems, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Nov 21, 2000 |
| Received | Aug 31, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002725
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.