Class Class II

HERA W10 Diagnostic Ultrasound System; HERA W9 Diagnostic Ultrasound System (K230084)

K230084 2023-04-21 Traditional
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Description

HERA W10 Diagnostic Ultrasound System; HERA W9 Diagnostic Ultrasound System by Samsung Medison Co., Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230084
Clearance Date2023-04-21
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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