Class Class II

PercuNav Image Fusion and Interventional Navigation System (K223804)

K223804 2023-01-18 Traditional
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Description

PercuNav Image Fusion and Interventional Navigation System by Philips Ultrasound, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223804
Clearance Date2023-01-18
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750

Categories

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