510(k) K922027 ยท DSI Detector And Alarm, Arrhythmia
AMBULATORY (HOLTER) RECORDING, MODIFICATION
| Applicant | Biosensor Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 17, 1993 |
| Received | Mar 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922027
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.