Class Class II

Lumify Diagnostic Ultrasound System (K252557)

K252557 2025-12-22 Traditional
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Description

Lumify Diagnostic Ultrasound System by Philips Ultrasound, LLC, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252557
Clearance Date2025-12-22
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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