Class Class II

EPIQ Series Diagnostic Ultrasound System (K231190)

K231190 2023-05-12 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK231190
Clearance Date2023-05-12
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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