510(k) K930095 ยท DSI Detector And Alarm, Arrhythmia
SPACELABS MEDICAL PATIENT MONITOR
| Applicant | Spacelabs Medical, Inc., Hamden CT, US |
| Decision | Substantially Equivalent, Sep 3, 1993 |
| Received | Jan 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930095
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.