Jkh USA, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K203636PlusCare Temperature Probes, Skin Types: PT2252-AS, PTHP-AS, PTMQ-AS, PTSW-AS, PTSM-15AS, PTSL-AS, PAugust 31, 2021
K203635Patient Monitoring CablesFebruary 5, 2021
K203652Blood Pressure Cuff, U1883S,U1883D, U1882S, U1882D, U1881S, U1881D, Blood Pressure Cuff, U1885S, U18January 6, 2021
K202851Spo2 SensorNovember 27, 2020
K201645Massage Compression BootsSeptember 15, 2020
K201470Disposable Medical Face MaskSeptember 8, 2020
K182671Medi-Direct TENS PenSeptember 21, 2019
K191151JKH Stimulator PlusJune 21, 2019
K182203JKH Stimulator PlusMarch 14, 2019