Class Class II

F&P Airvo 3 (K221338)

K221338 2023-01-27 Traditional
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Description

F&P Airvo 3 by Fisher & Paykel Health Care — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221338
Clearance Date2023-01-27
Clearance TypeTraditional
Product CodeQAV
Regulation Number868.5454

Categories

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