AMSTERDAM (dpa-AFX) - Koninklijke Philips Electronics NV (PHGFF.PK, PHG) said it received 510 (K) marketing clearance from U.S. Food and Drug Administration or FDA, for its innovative ultra mobile ultrasound system VISIQ.
VISIQ with its transducer-plus-tablet display delivers excellent image quality, making ultrasound available anytime, in a wide range of clinical environments for OB patients.
Currently, it is commercially available in China, East Africa, France, Germany and India.
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