ClearanceBrief
510(k) K792355 ยท DXQ Blood Pressure Cuff

ANEROID SPHYMOMANOMETER

ApplicantAbco Dealers, Inc., Walker MI, US
DecisionSubstantially Equivalent, Dec 5, 1979
ReceivedNov 21, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792355

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.