FDA 510(k) Applications for Medical Device Product Code "KTB"
(Device, Iontophoresis, Specific Uses)

FDA 510(k) Number Applicant Device Name Decision Date
K180627 ELITechGroup Inc. Macroduct Advanced Model 3710 07/27/2018
K974855 IOMED, INC. PHORESOR II, MODEL PM900 03/27/1998
K001410 IOMED, INC. PHORESOR MODEL PM2000 08/01/2000
K031115 IOMED, INC. RH-900 07/10/2003
K033192 IOMED, INC. RH-950 12/22/2003
K954126 IOMED, INC. TRANSQ ELECTRODE PHORESOR II 01/19/1996
K001522 IOMED, INC. TRANSQ3 10/18/2000
K031551 VYTERIS, INC. NORTHSTAR LIDOCAINE IONTOPHORETIC CONTROLLER (NORTHSTAR CONTROLLER-D) 08/20/2003
K010031 WESCOR, INC. NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM 03/20/2001
K992874 WR MEDICAL ELECTRONICS CO. Q-SWEAT QUANTITATIVE SWEAT MEASUREMENT SYSTEM 11/18/1999


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