510(k) K852270 ยท DSI Detector And Alarm, Arrhythmia
LIFESCOPE 8 DEC-8108A AND DEC-8204A
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jul 30, 1985 |
| Received | May 28, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852270
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.