510(k) K854115 ยท DSI Detector And Alarm, Arrhythmia
CUSTO PORT 24-H ECG AMBULATORY RECORDER
| Applicant | Versacor, Inc., Dayton OH, US |
| Decision | Substantially Equivalent, Jan 27, 1986 |
| Received | Oct 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854115
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.