510(k) K972498 ยท DSI Detector And Alarm, Arrhythmia
OBSERVER * CENTRAL STATION
| Applicant | Johnson & Johnson Medical, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Feb 17, 1998 |
| Received | Jul 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972498
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.