Jkh USA, LLC
Jkh USA, LLC holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2021.
Top product codes for Jkh USA, LLC
Recent clearances by Jkh USA, LLC
- K203636 — PlusCare Temperature Probes, Skin Types: PT2252-AS, PTHP-AS, PTMQ-AS, PTSW-AS, PTSM-15AS, PTSL-AS, PTMR-AS +1 more
- K203635 — Patient Monitoring Cables
- K203652 — 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,U1740S, U1750S, U1760S, Blood Pressure Cuff, U1770S, U1790s, U1710D, U1720D, U1730D, U1740D
- K202851 — Spo2 Sensor
- K201645 — Massage Compression Boots
- K201470 — Disposable Medical Face Mask
- K182671 — Medi-Direct TENS Pen
- K191151 — JKH Stimulator Plus
- K182203 — JKH Stimulator Plus
Data sourced from openFDA. This site is unofficial and independent of the FDA.