Class Class II

DeltaScan Monitor (K222680)

K222680 2023-02-02 Traditional
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Description

DeltaScan Monitor by Prolira B.V. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222680
Clearance Date2023-02-02
Clearance TypeTraditional
Product CodeNCG
Regulation Number882.1440

Categories

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