510(k) K021681 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MICROPAQ, MODELS 402, 404
| Applicant | Welch Allyn Protocol, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Jul 23, 2002 |
| Received | May 22, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021681
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.