FDA 510(k) Applications Submitted by Bill Quanqin Dai

FDA 510(k) Number Submission Date Device Name Applicant
K131921 06/26/2013 ELECTRONIC PULSE STIMULATOR SHENZHEN JINGKEHUI ELECTRONIC CO., LTD
K141260 05/15/2014 ELECTRONIC PULSE STIMULATOR SHENZHEN JINGKEHUI ELECTRONIC CO., LTD
K191151 05/01/2019 JKH Stimulator Plus JKH USA, LLC
K201470 06/03/2020 Disposable Medical Face Mask JKH USA, LLC
K201645 06/17/2020 Massage Compression Boots JKH USA, LLC
K182203 08/15/2018 JKH Stimulator Plus JKH USA, LLC
K182671 09/26/2018 Medi-Direct TENS Pen JKH USA, LLC
K202851 09/28/2020 Spo2 Sensor JKH USA, LLC
K203635 12/14/2020 Patient Monitoring Cables JKH USA, LLC
K203636 12/14/2020 PlusCare Temperature Probes, Skin Types: PT2252-AS, PTHP-AS, PTMQ-AS, PTSW-AS, PTSM-15AS, PTSL-AS, PTMR-AS; Rectum Types: PT2252-AG, PTHP-AG, PTMQ-AG, PTSW-AG, PTSM-15AG, PTSL-AG, PTMR-AG JKH USA, LLC
K203652 12/14/2020 Blood Pressure Cuff, U1883S,U1883D, U1882S, U1882D, U1881S, U1881D, Blood Pressure Cuff, U1885S, U1885D, U1880S, U1880D, U1886S, U1886D, Blood Pressure Cuff, U1869S, U1869D, U1889S, U1889D, U1884S, U1884D, Blood Pressure Cuff, U1710S, U1720S, U1730S,U1740 JKH USA, LLC


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact