Philips Medical Systems North America Co.
FDA 510(k) medical device clearances.
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.