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FDA 510(k) Applications for Medical Device Product Code "KTB"
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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 |