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Live View Panel Version 1.4

by Neurotronics, LLC

Live View Panel Version 1.4 is a Class II device made by Neurotronics, LLC, cleared under FDA 510(k) K131415 on 9 Aug 2013 and listed in FDA GUDID since 5 Oct 2017 (UDI-DI 00817111020816), active as of 21 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 21 Oct 2026

Documents

510(k) K131415

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817111020816 UDI-DI Date5 Oct 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK131415 Date9 Aug 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131415 decided 9 Aug 2013 Active
  • FDA GUDID UDI-DI 00817111020816 listed 5 Oct 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131415
  2. Listed FDA GUDID 00817111020816

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Generic name
Bioelectrical signal analysis software
Model / reference
1.4
Primary DI / UDI-DI
00817111020816
510(k) Number
FDA product code
GWQ, OLT, OLV, OLZ
GMDN term
Bioelectrical signal analysis software
Device class
Class II
Regulation number
882.1400
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GWQ (Full-Montage Standard Electroencephalograph).

Other devices from Neurotronics, LLC

See all devices from Neurotronics, LLC →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)