ClearanceBrief
510(k) K781591 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

NEBULIZER/HUMIDIFIER MODEL EH 147B

ApplicantMistogen Equipment Co., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 16, 1978
ReceivedSep 18, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781591

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.