510(k) K932620

RH-806/GS MODEL TRANSQ(R)2 by Iomed, Inc. — Product Code EGJ

K932620 is an FDA 510(k) premarket notification submitted by Iomed, Inc. for the device "RH-806/GS MODEL TRANSQ(R)2". The FDA issued a decision of Substantially Equivalent on July 26, 1994. The device falls under product code EGJ (Device, Iontophoresis, Other Uses), a Class II device regulated under 21 CFR 890.5525. Iomed, Inc. has at least 10 other 510(k) clearances on record.