ClearanceBrief
510(k) K802852 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

HUMIDIFIER

ApplicantAirlife, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 26, 1981
ReceivedNov 12, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802852

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.