Philips Medical Systems North America Co.
Philips Medical Systems North America Co. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2010.
Top product codes for Philips Medical Systems North America Co.
Recent clearances by Philips Medical Systems North America Co.
- K101311 — EP NAVIGATOR R3
- K090625 — WIRELESS PORTABLE DETECTOR FD-W17
- K090590 — VERADIUS, MODEL 718-130
- K082280 — SURESIGNS VS2 VITAL SIGNS MONITOR, SURESIGNS VM1 PATIENT MONITOR, SURESIGNS VS3 CITAL SIGNS MONITOR
- K063781 — PHILIPS XD-S DIRECT RADIOGRAPHY WORKSTATION/PACKAGE
- K062268 — MASIMO SET SPO2 MODULE FOR PHILIPS AND M3001A MULTI-MEASUREMENT SERVER OPTION A03
- K061685 — PULSERA
- K061995 — XCELERA
- K060749 — XPERCT
- K050692 — FLXIS
- K043147 — ACHIEVA FAMILY
- K042368 — PRACTIX CONVENIO
- K042334 — ALLURA 3D-CA, RELEASE 1
- K041949 — ALLURA XPER FD10
- K040254 — INTEGRIS 3D-RA, RELEASE 4.2
- K031836 — PHILIPS FRESCO RELEASE 1
- K031597 — DUNLEE FORMAT COLLIMATOR FAMILY
- K031535 — PHILIPS EASYDIAGNOST ELEVA
- K030520 — INTERA FAMILY
- K023137 — PHILIPS EASYVISION WORKSTATION RELEASE 6
- K022899 — PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0
- K022788 — PHILIPS HARMONY RELEASE 1
- K013344 — INTERA I/T
- K012238 — DOSERIGHT
Data sourced from openFDA. This site is unofficial and independent of the FDA.