510(k) K895266 ยท DSI Detector And Alarm, Arrhythmia
AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED
| Applicant | Biosensor Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 26, 1990 |
| Received | Aug 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895266
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.