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Nicolet Wireless EEG

by Carefusion 209, Inc.

510(k) K103140

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 9 Oct 2026. What this means

Regulatory status

as of registry sync 9 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK103140 Date8 Apr 2011ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0946-2013 FDA Class II initiated 27 Feb 2013

    Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier which may overheat and become uncomfortable to touch around the area of the on/off button. The overheating may result in discomfort ranging from too hot up to the potential for a burn.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
GWL
Device Class
Class II
Regulation
21 CFR Part 882.1835
Advisory Committee
Neurology
FDA Decision
SESE Substantially Equivalent

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