ClearanceBrief
510(k) K851220 ยท KFZ Humidifier, Non-Direct Patient Interface (Home-Use)

SUNBEAM EVAPORATIVE HUMIDIFIER 663 & 664

ApplicantNorthern Electric Co. Div. of Sunbeam Corp., Chicago IL, US
DecisionSubstantially Equivalent, Sep 17, 1985
ReceivedMar 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851220

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.