510(k) K874965

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE by Solway, Inc. — Product Code HTD

K874965 is an FDA 510(k) premarket notification submitted by Solway, Inc. for the device "MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE". The FDA issued a decision of Substantially Equivalent on December 30, 1987. The device falls under product code HTD (Forceps), a Class I device regulated under 21 CFR 878.4800. Solway, Inc. has at least 10 other 510(k) clearances on record.