510(k) K760593 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PORTABLE CARDIAC MONITOR, ABBY
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Sep 16, 1976 |
| Received | Sep 7, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760593
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.