510(k) K881488 ยท DSI Detector And Alarm, Arrhythmia
HOLTER SCANNER
| Applicant | Cardiodata Corp., Northborough MA, US |
| Decision | Substantially Equivalent, Sep 20, 1988 |
| Received | Apr 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881488
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.