Medical Device Manufacturer · US , North Attleboro , MA

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

18 submissions · 17 cleared · Since 1998

Total

Cleared

Denied

Neurometrix, Inc. has 17 FDA 510(k) cleared neurology devices. Based in North Attleboro, US.

Historical record: 17 cleared submissions from 1998 to 2016.

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 - Neurometrix, Inc.

18 devices

1-18 of 18

Not Cleared May 18, 2022

Anesthesiology · 135d

Cleared May 27, 2009

NEUROMETRIX BIOAMPLIFIER

MODIFICATION TO NC-STAT

K041320 · JXE

Neurology · 86d

Cleared Jan 17, 2002

MODIFICATION OF NC-STAT

MODIFICATION TO NC-STAT

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

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

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