510(k) K960544 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
CARDIO-CARD HOLTER ECG MANAGEMENT SYSTEM
| Applicant | Nasiff Assoc., Inc., Brewerton NY, US |
| Decision | Substantially Equivalent, Aug 7, 1996 |
| Received | Feb 7, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960544
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.