Class Class II

Neurophet AQUA AD Plus (K252496)

K252496 2026-01-29 Traditional
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Description

Neurophet AQUA AD Plus by Neurophet., Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252496
Clearance Date2026-01-29
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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