Class Class II

Revitalair 430+ (K220290)

K220290 2023-05-04 Traditional
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Description

Revitalair 430+ by Us Hyperbaric Network — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220290
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeCBF
Regulation Number868.5470

Categories

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