510(k) K012451 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246
| Applicant | Welch Allyn Protocol, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Aug 20, 2001 |
| Received | Aug 1, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012451
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.