ClearanceBrief
510(k) K921143 ยท FQO Table, Operating-Room, Ac-Powered

PNEUMO-WEDGE

ApplicantKansas Creative Devices, Inc., Laewood KS, US
DecisionSubstantially Equivalent, Sep 11, 1992
ReceivedMar 11, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921143

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.