ClearanceBrief
510(k) K192500 ยท DXQ Blood Pressure Cuff

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer

ApplicantHonsun (Nantong) Co., Ltd., Nantong, CN
DecisionSubstantially Equivalent, Apr 6, 2020
ReceivedSep 12, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192500

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.