510(k) K914576 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
KELLER CARDIAC MONITOR MEDIL KMS870
| Applicant | Keller Medical Specialties Products, Inc., Antioch IL, US |
| Decision | Substantially Equivalent, Dec 30, 1991 |
| Received | Oct 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914576
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.