510(k) K960884 ยท DSI Detector And Alarm, Arrhythmia
TELE TRENS TM 10
| Applicant | Life Sensing Instrument Company, Inc., Tullahoma TN, US |
| Decision | Substantially Equivalent, Sep 12, 1997 |
| Received | Mar 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960884
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.