Class Class II

Lumify Diagnostic Ultrasound System (K223771)

K223771 2023-05-04 Traditional
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Description

Lumify Diagnostic Ultrasound System by Philips Ultrasound — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223771
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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