Jkh USA, LLC
FDA 510(k) & PMA Approved Devices — 9 products
Total Devices9
Categories7
Latest Approval2021-08-31
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 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-AG | FLL | 2021-08-31 | View |
| 510(k) | K203635 | Patient Monitoring Cables | DSA | 2021-02-05 | 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, U1740D | DXQ | 2021-01-06 | View |
| 510(k) | K202851 | Spo2 Sensor | DQA | 2020-11-27 | View |
| 510(k) | K201645 | Massage Compression Boots | IRP | 2020-09-15 | View |
| 510(k) | K201470 | Disposable Medical Face Mask | FXX | 2020-09-08 | View |
| 510(k) | K182671 | Medi-Direct TENS Pen | NUH | 2019-09-21 | View |
| 510(k) | K191151 | JKH Stimulator Plus | NUH | 2019-06-21 | View |
| 510(k) | K182203 | JKH Stimulator Plus | NUH | 2019-03-14 | View |
No matching devices.