Medical Device Manufacturer · US , Walker , MI

Cadwell Laboratories, Inc. - FDA 510(k) Cleared Devices

46 submissions · 46 cleared · Since 1979

Total

Cleared

Denied

Cadwell Laboratories, Inc. has 46 FDA 510(k) cleared neurology devices. Based in Walker, US.

Historical record: 46 cleared submissions from 1979 to 2007.

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

FDA 510(k) Regulatory Record - Cadwell Laboratories, Inc.

46 devices

1-12 of 46

Cleared Mar 05, 2007

CADWELL EASYNET OXIMETER MODULE

K061706 · DQA

Anesthesiology · 262d

Cleared Nov 21, 2006

CADWELL EASYNET NASAL PRESSURE MODULE

K061705 · MNR

Anesthesiology · 158d

Cleared Nov 03, 2004

TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATOR

K042350 · GWF

Neurology · 65d

Cleared Jul 01, 2004

EASYNET BODY POSITION MODULE

K040932 · LEL

Neurology · 83d

Cleared Jul 01, 2004

CADWELL LIMB MOVEMENT MODULE

FOUR-CHANNEL PREAMPLIFIER

K962455 · GWF

Neurology · 202d

Cleared Jan 13, 1997

TWO-CHANNEL PREAMPLIFIER

K962457 · GWF

Neurology · 202d

Cleared Jan 13, 1997

CADWELL FOUR-/EIGHT-CHANNEL PREAMPLIFIER

K962458 · GWF

Neurology · 202d

Cleared Sep 12, 1995

CADWELL EASY AMBULATORY EEG

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Cadwell Laboratories, Inc. - FDA 510(k) Cleared Devices

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