510(k) K240165 ยท DXQ Blood Pressure Cuff
Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer
| Applicant | Wenzhou Longwan Medical Device Factory, Wenzhou, CN |
| Decision | Substantially Equivalent, Mar 20, 2024 |
| Received | Jan 22, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240165
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.