FDA 510(k) Applications Submitted by IOMED, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K954126 |
09/01/1995 |
TRANSQ ELECTRODE PHORESOR II |
IOMED, INC. |
K060236 |
01/30/2006 |
MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE |
IOMED, INC. |
K031115 |
04/08/2003 |
RH-900 |
IOMED, INC. |
K033192 |
10/02/2003 |
RH-950 |
IOMED, INC. |
K063465 |
11/16/2006 |
CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE |
IOMED, INC. |
K001410 |
05/04/2000 |
PHORESOR MODEL PM2000 |
IOMED, INC. |
K001522 |
05/16/2000 |
TRANSQ3 |
IOMED, INC. |
K974855 |
12/29/1997 |
PHORESOR II, MODEL PM900 |
IOMED, INC. |
K982668 |
07/31/1998 |
PHORESOR II,MODEL PM900 |
IOMED, INC. |
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