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Beijing Choice Electronic Technology Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232975Pulse Oximeter (MD300C228)June 21, 2024
K230587Wrist Pulse OximeterNovember 30, 2023
K230172Pulse OximeterAugust 12, 2023
K220101Pulse OximeterMarch 8, 2023
K221992Electronic Pulse StimulatorOctober 21, 2022
K211400Pulse OximeterFebruary 11, 2022
K211752Infrared ThermometerJanuary 21, 2022
K211754Vital Signs MonitorNovember 15, 2021
K181503Fingertip Pulse OximeterOctober 11, 2018
K172366Wrist Pulse OximeterMarch 16, 2018
K162089Blood Pressure MonitorFebruary 10, 2017
K160268Fingertip Pulse Oximeter MD300CG11/MD300CG51October 14, 2016
K161560Fingertip Pulse Oximeter MD300CN310October 5, 2016
K152563Pulse Oximeter (MD300M/MD300K2)April 18, 2016