Philips Medical Systems
Philips Medical Systems holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2021, with 16 FDA device recalls on record.
Clearances by Philips Medical Systems — page 2
101–107 of 107- K021251 — ST/AR ST AND ARRHYTHMIA SOFTWARE, RELEASE E.I.
- K021347 — MODIFICATION TO M2376A DEVICELINK SYSTEM
- K020531 — PHILIPS MULTI-PARAMETER MODULE, MODEL M3001A; PHILIPS COMPONENT COMPACT MONITOR, RELEASE A.02, MODEL M1275B
- K020055 — PHILIPS INTEGRIS ALLURA 9 WITH FD OPTION
- K014157 — HEARTSTREAMFR2 AED WITH M3848A AND M3849A, MODELS M3860A, M3861, M3840A, M3841A
- K013425 — HEARTSTREAM/HEARTSTART FR2 AED ECG CABLE, MODELS M3860A, M3861A, M3840A, M3841A
- K014191 — M2540 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL M2540
Data sourced from openFDA. This site is unofficial and independent of the FDA.