510(k) K033646 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
TRIFIT 700
| Applicant | Healthfirst Corp., Albuquerque NM, US |
| Decision | Substantially Equivalent, Mar 1, 2005 |
| Received | Nov 20, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033646
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.