Class Class II

Wesper Lab (K221816)

K221816 2023-03-09 Traditional
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Description

Wesper Lab by Wesper, Inc. — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221816
Clearance Date2023-03-09
Clearance TypeTraditional
Product CodeMNR
Regulation Number868.2375

Categories

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