Medical Device Manufacturer · US , Mchenry , IL

Chattanooga Group, Inc. - FDA 510(k) Cleared Devices

70 submissions · 68 cleared · Since 1980

Total

Cleared

Denied

Chattanooga Group, Inc. has 68 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 68 cleared submissions from 1980 to 2001. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Chattanooga Group, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Chattanooga Group, Inc.

70 devices

1-12 of 70

Cleared Jul 06, 2001

CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000

K011243 · LSB

Physical Medicine · 74d

Cleared Feb 01, 1999

VECTRA COMBO

K982317 · IMG

Physical Medicine · 214d

Cleared Feb 01, 1999

VECTRA STIM MODELS 200 AND 400

K982321 · GZJ

Neurology · 214d

Cleared Feb 01, 1999

VECTRA PRO MODELS 2 AND 4

K982324 · GZJ

Neurology · 214d

Cleared Nov 06, 1998

FORTE, MODELS CPS 400 STIM, CPS 200 STIM

K982828 · IPF

Physical Medicine · 87d

Cleared Nov 06, 1998

FORTE, MODEL CPS ULTRASOUND

K982829 · IMI

Physical Medicine · 87d

Cleared Nov 06, 1998

FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO

K982830 · IMG

Physical Medicine · 87d

Cleared Mar 27, 1998

PARA-CARE

K980718 · IMC

Physical Medicine · 31d

INTELECT LEGEND ULTRASOUND

K973024 · IMI

Physical Medicine · 88d

Physical Medicine · 85d

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Chattanooga Group, Inc. - FDA 510(k) Cleared Devices

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