Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Jkh USA, LLC

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories7
Latest FDA decision2021-08-31
TypeNumberDevice NameCodeDateActions
510(k) K203636 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-AGFLL2021-08-31 View
510(k) K203635 Patient Monitoring CablesDSA2021-02-05 View
510(k) 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, U1740DDXQ2021-01-06 View
510(k) K202851 Spo2 SensorDQA2020-11-27 View
510(k) K201645 Massage Compression BootsIRP2020-09-15 View
510(k) K201470 Disposable Medical Face MaskFXX2020-09-08 View
510(k) K182671 Medi-Direct TENS PenNUH2019-09-21 View
510(k) K191151 JKH Stimulator PlusNUH2019-06-21 View
510(k) K182203 JKH Stimulator PlusNUH2019-03-14 View