Philips Medical Systems, Inc.
Philips Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2010, with 65 FDA device recalls on record.
Clearances by Philips Medical Systems, Inc. — page 2
101–111 of 111- K882022 — TOMOSCAN LX COMPUTED TOMOGRAPHY SYSTEM
- K874558 — SL SERIES, SL 15, 18, 20 & 25
- K880822 — PICS-2000
- K854654 — SM PART SERVO SEC. DUPLEX DOP 7-5/5 9814-219-50007
- K860234 — TRANSVAGINAL TRANSDUCER, 5MHZ
- K854590 — HANDHELD DOPLER/PEN TRANSDUCER 3MHZ
- K854591 — SUPRASTERNAL NOTCH DOP/TRANS. 3MHZ
- K844772 — 6.0 MHZ LA6060 TRANSDUCER & 4.0 MHZ LA4011 TRANSDU
- K852768 — ORALIX PANORAMIC D.C.
- K842900 — PHILIPS SDR 1200
- K833226 — PMX MOBILE X-RAY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.