510(k) K203652 ยท DXQ Blood Pressure Cuff
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, U1770
| Applicant | Jkh USA, LLC, Walnut CA, US |
| Decision | Substantially Equivalent, Jan 6, 2021 |
| Received | Dec 14, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203652
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.