Brief: Philips Receives FDA 510(K) Clearance For Its Rembra Platform

Koninklijke Philips

22/04/2026 14:02

April 22 (Reuters) - Koninklijke Philips NV PHG.AS:

PHILIPS RECEIVES FDA 510(K) CLEARANCE FOR ITS REMBRA PLATFORM, EXPANDING ACCESS TO FASTER, MORE PRECISE CT IMAGING ACROSS FRONTLINE CARE AND CANCER TREATMENT PLANNING

Source text: ID:nGNX9vyLmd

Further company coverage: PHG.AS

 (Gdansk Newsroom)

 ((gdansk.newsroom@thomsonreuters.com; +48 58 769 66 00;))