510(k) K021300 ยท DSI Detector And Alarm, Arrhythmia
MODIFICATION OF PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.03, MODEL M1275B
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, May 8, 2002 |
| Received | Apr 24, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021300
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.