ClearanceBrief
510(k) K871271 ยท DRM Compressor, Cardiac, External

HUNTLEIGH FLOWPRESS AC300 PUMP, SQ301/302/320 GAR.

ApplicantHuntleigh Technology, Inc., Manalapan NJ, US
DecisionSubstantially Equivalent, Sep 15, 1987
ReceivedMar 31, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871271

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.