ClearanceBrief
510(k) K924732 ยท FYD Apparatus, Exhaust, Surgical

PORTA PLUMESAFE(TM) 601 SMOKE EVACUATION SYSTEM

ApplicantBuffalo Filter Co., Inc., E. Amherst NY, US
DecisionSubstantially Equivalent, Sep 13, 1993
ReceivedSep 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924732

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.