Jkh USA, LLC
FDA 510(k) & PMA Approved Dispositivos — 9 products
Publicidade
Total de dispositivos9
Categorias0
Última decisão da FDA
| Tipo | Número | Nome do dispositivo | Código | Data | Ações |
|---|---|---|---|---|---|
| 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 | Ver |
| 510(k) | K203635 | Patient Monitoring Cables | DSA | 2021-02-05 | Ver |
| 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 | Ver |
| 510(k) | K202851 | Spo2 Sensor | DQA | 2020-11-27 | Ver |
| 510(k) | K201645 | Massage Compression Boots | IRP | 2020-09-15 | Ver |
| 510(k) | K201470 | Disposable Medical Face Mask | FXX | 2020-09-08 | Ver |
| 510(k) | K182671 | Medi-Direct TENS Pen | NUH | 2019-09-21 | Ver |
| 510(k) | K191151 | JKH Stimulator Plus | NUH | 2019-06-21 | Ver |
| 510(k) | K182203 | JKH Stimulator Plus | NUH | 2019-03-14 | Ver |
Nenhum dispositivo correspondente.