ClearanceBrief
510(k) K800056 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

VENTILATOR SET

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Jan 24, 1980
ReceivedJan 10, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800056

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.