ClearanceBrief
510(k) K930041 ยท FYD Apparatus, Exhaust, Surgical

VICROSAFE 6 AND VICROSAFE 12

ApplicantBuffalo Filter Co., Inc., E. Amherst NY, US
DecisionSubstantially Equivalent, Nov 3, 1993
ReceivedJan 5, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930041

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.