Class Class II

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System (K251651)

K251651 2025-10-09 Special
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Description

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System by Philips Ultrasound, LLC, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251651
Clearance Date2025-10-09
Clearance TypeSpecial
Product CodeIYN
Regulation Number892.1550

Categories

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