Class Class II

TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US) (K230136)

K230136 2023-04-24 Traditional
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Description

TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US) by Compai Healthcare (Suzhou) Co.,Ltd — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230136
Clearance Date2023-04-24
Clearance TypeTraditional
Product CodeMWP
Regulation Number892.1680

Categories

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