510(k) K014159 ยท DSI Detector And Alarm, Arrhythmia
PHILLIPS M1175A/76A/77A COMPONENT MONITORING SYSTEM; PHILLIPS V24/V26 PATIENT MONITOR
| Applicant | Philips Medical Systems, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jan 18, 2002 |
| Received | Dec 19, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014159
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.