510(k) K771701

VESSEL-CLUDE by Med General — Product Code GDJ

K771701 is an FDA 510(k) premarket notification submitted by Med General for the device "VESSEL-CLUDE". The FDA issued a decision of Substantially Equivalent on December 13, 1977. The device falls under product code GDJ (Clamp, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. Med General has at least 10 other 510(k) clearances on record.