ClearanceBrief
510(k) K922555 ยท FYD Apparatus, Exhaust, Surgical

ENVIROMATE(TM) SMOKE EVACUATION SYSTEM

ApplicantLase, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jan 6, 1993
ReceivedMay 29, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922555

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.