510(k) K861471

V. MUELLER VITAL CLIP-HEMOSTATIC CLIP by American V. Mueller — Product Code FZP

K861471 is an FDA 510(k) premarket notification submitted by American V. Mueller for the device "V. MUELLER VITAL CLIP-HEMOSTATIC CLIP". The FDA issued a decision of Substantially Equivalent on June 6, 1986. The device falls under product code FZP (Clip, Implantable), a Class II device regulated under 21 CFR 878.4300. American V. Mueller has at least 10 other 510(k) clearances on record.