Class Class II

Fingertip Pulse Oximeter (K213430)

K213430 2022-12-30 Traditional
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Description

Fingertip Pulse Oximeter by Shenzhen Witleaf Medical Electronics Co., Ltd. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213430
Clearance Date2022-12-30
Clearance TypeTraditional
Product CodeDQA
Regulation Number870.2700

Categories

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