510(k) K841500 ยท DSI Detector And Alarm, Arrhythmia
LIFESCOPE 6 OEC-6201
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Aug 28, 1984 |
| Received | Apr 10, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841500
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.