FDA 510(k) Applications Submitted by BILL 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 |
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