FDA 510(k) Applications Submitted by Shenzhen Smallsignal Technology Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K232520 08/18/2023 Fingertip Pulse Oximeter, models Alpine20, Alpine20A, Alpine20H, Alpine20HA, Alpine20B, Alpine20BA, Alpine20BH, Alpine20BHA, Alpine30, Alpine30A, Alpine30H, Alpine30HA, Alpine30B, Alpine30BA, Alpine30BH, Alpine30BHA, Alpine20L, Alpine20LB, Alpine20LH, Alp Shenzhen Smallsignal Technology Co., Ltd.


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