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Iomed, Inc.

17 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE (K063465)Iomed, Inc.2007-02-28
MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE (K060236)Iomed, Inc.2006-03-31
RH-950 (K033192)Iomed, Inc.2003-12-22
RH-900 (K031115)Iomed, Inc.2003-07-10
TRANSQ3 (K001522)Iomed, Inc.2000-10-18
PHORESOR MODEL PM2000 (K001410)Iomed, Inc.2000-08-01
PHORESOR II,MODEL PM900 (K982668)Iomed, Inc.1999-03-02
PHORESOR II, MODEL PM900 (K974855)Iomed, Inc.1998-03-27
TRANSQ ELECTRODE PHORESOR II (K954126)Iomed, Inc.1996-01-19
RH-801/GS MODEL TRANSQ(R)1 (K932621)Iomed, Inc.1994-07-26
PHORESOR II AUTO, MODEL PM800 MODIFICATION (K934335)Iomed, Inc.1994-07-26
RH-806/GS MODEL TRANSQ(R)2 (K932620)Iomed, Inc.1994-07-26
RH-801, MODEL TRANSQ (K925806)Iomed, Inc.1994-07-14
RH-806, MODEL TRANSQ (K925800)Iomed, Inc.1994-07-14
IONTOPHORESIS DEVICE, MODIFICATION (K914621)Iomed, Inc.1991-12-20
TRANSQ 2 (K914264)Iomed, Inc.1991-12-20
IONTOPHORESIS DEVICE - ELECTRODE RH 800 (K896444)Iomed, Inc.1990-05-10

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