FDA 510(k) Applications Submitted by Shenzhen Witleaf Medical Electronics Co.,Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K213430 10/21/2021 Fingertip Pulse Oximeter Shenzhen Witleaf Medical Electronics Co.,Ltd
K213431 10/21/2021 Handheld Pulse Oximeter Shenzhen Witleaf Medical Electronics Co.,Ltd


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