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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