FDA 510(k) Applications Submitted by JKH HEALTH CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K211050 04/08/2021 Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304 JKH HEALTH CO., LTD.
K162517 09/09/2016 Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13 JKH Health Co., Ltd.
K202839 09/25/2020 Overlapped Compression Therapy JKH HEALTH CO., LTD.


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