ClearanceBrief
510(k) K810009 ยท DRS Transducer, Blood-Pressure, Extravascular

DISPOSABLE DIAPHRAGM DOME

ApplicantMedex, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 19, 1981
ReceivedJan 5, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810009

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.