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Shenzhen Jumper Medical Equipment Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231310Electronic Blood Pressure MonitorOctober 27, 2023
K182871Mini TENS Therapy DeviceAugust 1, 2019
K182437Wireless Intelligent ThermometerMay 5, 2019
K182495Electronic Blood Pressure MonitorMarch 3, 2019
K172795Infrared ThermometerMarch 14, 2018
K170965Fingertip Pulse OximeterNovember 3, 2017
K140582FINGERTIP PULSE OXIMETERAugust 28, 2014
K131457FETAL ULTRASONIC MONITOR AND ACCESSORIESJanuary 24, 2014
K131243NON-CONTACT INFRARED THERMOMETERNovember 12, 2013
K110124FETAL DOPPLER JPD-100SFebruary 4, 2011