510(k) K913339 ยท DSI Detector And Alarm, Arrhythmia
HORIZON PACEMAKER DETECTION SOFTWARE
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Jan 8, 1992 |
| Received | Jul 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913339
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.