510(k) K842737

CARNOY'S SOLUTION by E K Ind., Inc. — Product Code IGM

K842737 is an FDA 510(k) premarket notification submitted by E K Ind., Inc. for the device "CARNOY'S SOLUTION". The FDA issued a decision of Substantially Equivalent on September 7, 1984. The device falls under product code IGM (Solution, Carnoy'S), a Class I device regulated under 21 CFR 864.4010. E K Ind., Inc. has at least 10 other 510(k) clearances on record.