510(k) K221857 ยท DXQ Blood Pressure Cuff
Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201
| Applicant | Zhejiang Lude Technology Development Co., Ltd., Wenzhou, CN |
| Decision | Substantially Equivalent, Oct 13, 2022 |
| Received | Jun 27, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221857
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.