ClearanceBrief
510(k) K230859 ยท DXQ Blood Pressure Cuff

Aneroid Sphygmomanometer

ApplicantWenzhou Kangshun Medical Devices Co.,Ltd, Wenzhou City, CN
DecisionSubstantially Equivalent, Jun 28, 2023
ReceivedMar 29, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230859

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.