ClearanceBrief
510(k) K871272 ยท DRM Compressor, Cardiac, External

HUNTLEIGH FLOWPAC FP2000

ApplicantHuntleigh Technology, Inc., Manalapan NJ, US
DecisionSubstantially Equivalent, Jun 25, 1987
ReceivedMar 31, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871272

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.