510(k) K885085 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ERGOMED 840/ERGOMED 840L
| Applicant | Burdick Corp., Miltoon WI, US |
| Decision | Substantially Equivalent, Oct 3, 1989 |
| Received | Dec 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885085
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.