510(k) K930041

VICROSAFE 6 AND VICROSAFE 12 by Buffalo Filter Co., Inc. — Product Code FYD

K930041 is an FDA 510(k) premarket notification submitted by Buffalo Filter Co., Inc. for the device "VICROSAFE 6 AND VICROSAFE 12". The FDA issued a decision of Substantially Equivalent on November 3, 1993. The device falls under product code FYD (Apparatus, Exhaust, Surgical), a Class II device regulated under 21 CFR 878.5070. Buffalo Filter Co., Inc. has at least 10 other 510(k) clearances on record.