ClearanceBrief
510(k) K760341 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

HUMIDIFIER, ELECTRONIC (EH147)

ApplicantMistogen Equipment Co., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 11, 1976
ReceivedJul 30, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760341

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.