510(k) K896967 ยท DSI Detector And Alarm, Arrhythmia
HTS 820 CARDIAC MONITOR
| Applicant | Life Sensing Instrument Company, Inc., Tullahoma TN, US |
| Decision | Substantially Equivalent, Mar 19, 1990 |
| Received | Dec 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896967
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.