510(k) K803223 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ADVANCMED ELIMINATOR
| Applicant | American Edwards Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 13, 1981 |
| Received | Dec 19, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803223
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.