Philips Medical Systems Nederland B.V.
Philips Medical Systems Nederland B.V. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2026, with 201 FDA device recalls on record.
Clearances by Philips Medical Systems Nederland B.V. — page 2
101–107 of 107- K121296 — INTERVENTIONAL WORKSPOT
- K121781 — ECHONAVIGATOR RELEASE 1
- K111245 — HEARTNAVIGATOR RELEASE 1
- K102344 — MDIXON SOFTWARE OPTION FOR INTERA 1.5T, ACHIEVA 1.5T & ACHIEVA 3.0T MR SYSTEMS
- K083740 — MAMMODIAGNOST VU
- K052078 — ACHIEVA, INTERA AND PANORAMA 1.0 RELEASE 2-SERIES
- K052013 — ACHIEVA 1.5T & INERA 1.5T FAMILY
Data sourced from openFDA. This site is unofficial and independent of the FDA.