Medical Device Manufacturer · US , Salt Lake City , UT

Iomed, Inc. - FDA 510(k) Cleared Devices

17 submissions · 12 cleared · Since 1990

Total

Cleared

Denied

Iomed, Inc. has 12 FDA 510(k) cleared physical medicine devices. Based in Salt Lake City, US.

Historical record: 12 cleared submissions from 1990 to 2007.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

Iomed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Iomed, Inc.

17 devices

1-12 of 17

Cleared Feb 28, 2007

CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE

K063465 · EGJ

Physical Medicine · 104d

Cleared Mar 31, 2006

MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE

K060236 · EGJ

Physical Medicine · 60d

Cleared Dec 22, 2003

RH-950

K033192 · KTB

Physical Medicine · 81d

Cleared Jul 10, 2003

RH-900

K031115 · KTB

Physical Medicine · 93d

Cleared Oct 18, 2000

TRANSQ3

K001522 · KTB

Physical Medicine · 155d

Cleared Aug 01, 2000

PHORESOR MODEL PM2000

K001410 · KTB

Physical Medicine · 89d

Cleared Mar 02, 1999

PHORESOR II,MODEL PM900

K982668 · EGJ

Physical Medicine · 214d

Cleared Mar 27, 1998

PHORESOR II, MODEL PM900

K974855 · KTB

Physical Medicine · 88d

Cleared Jan 19, 1996

TRANSQ ELECTRODE PHORESOR II

K954126 · KTB

Physical Medicine · 140d

Cleared Jul 26, 1994

RH-806/GS MODEL TRANSQ(R)2

K932620 · EGJ

Physical Medicine · 420d

Cleared Jul 26, 1994

RH-801/GS MODEL TRANSQ(R)1

K932621 · EGJ

Physical Medicine · 420d

Cleared Jul 26, 1994

PHORESOR II AUTO, MODEL PM800 MODIFICATION

K934335 · EGJ

Physical Medicine · 322d

Iomed, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Iomed, Inc.

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