Class Class II

Neurophet AQUA (K220437)

K220437 2023-05-10 Traditional
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Description

Neurophet AQUA by Neurophet., Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220437
Clearance Date2023-05-10
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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