Class Class II

F&P Optiflow Flow Diverter (K234053)

K234053 2024-08-09 Traditional
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Description

F&P Optiflow Flow Diverter by Fisher &Paykel Healthcare , Ltd. — FDA 510(k) cleared anesthesiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234053
Clearance Date2024-08-09
Clearance TypeTraditional
Product CodeCBP
Regulation Number868.5870

Categories

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