Class Class II

Pulse Oximeter (K220101)

K220101 2023-03-08 Traditional
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Description

Pulse Oximeter by Beijing Choice Electronic Technology Co., Ltd. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220101
Clearance Date2023-03-08
Clearance TypeTraditional
Product CodeDQA
Regulation Number870.2700

Categories

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