510(k) K900246 ยท DSI Detector And Alarm, Arrhythmia
CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512
| Applicant | Ppg Industries, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Jul 3, 1990 |
| Received | Jan 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900246
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.