510(k) K946162

3M(TM) SURGICAL SLIPPER, 9660 SERIES by Wahl Clipper Corp. — Product Code LWK

K946162 is an FDA 510(k) premarket notification submitted by Wahl Clipper Corp. for the device "3M(TM) SURGICAL SLIPPER, 9660 SERIES". The FDA issued a decision of Substantially Equivalent on January 24, 1995. The device falls under product code LWK (Razor, Surgical), a Class I device regulated under 21 CFR 878.4800. Wahl Clipper Corp. has at least 7 other 510(k) clearances on record.