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510(k) K081741

NEUROLINK IP, MODEL PK1113 by Excel-Tech Ltd. (Xltek) — Product Code GWQ

K081741 is an FDA 510(k) premarket notification submitted by Excel-Tech Ltd. (Xltek) for the device "NEUROLINK IP, MODEL PK1113". The FDA issued a decision of Substantially Equivalent on October 31, 2008. The device falls under product code GWQ (Full-Montage Standard Electroencephalograph), a Class II device regulated under 21 CFR 882.1400. Excel-Tech Ltd. (Xltek) has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 2008
Date Received
June 19, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Full-Montage Standard Electroencephalograph
Device Class
Class II
Regulation Number
882.1400
Review Panel
NE
Submission Type

Acquire, display, store, and archive electroencephalographic signals from the brain using a full montage array (i.e., 16 or more electrodes) and user-specified locations

Other clearances by Excel-Tech Ltd. (Xltek)

  • K131266 — TREZ_HD (February 14, 2014)
  • K123079 — OLYMPIC BRAINZ MONITOR (May 8, 2013)
  • K120260 — ICTA (June 29, 2012)
  • K090277 — NATUS SLEEPWORKS, MODEL 104017 (April 19, 2011)
  • K100126 — STELLATE GRIDVIEW (December 3, 2010)

Other clearances for product code GWQ

  • K261604 — Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32) (June 13, 2026)
  • K260455 — New Wave System (March 13, 2026)
  • K233403 — Flexset System (April 30, 2024)
  • K231366 — Neuronaute Plus (November 9, 2023)
  • K221959 — Q21 (August 31, 2023)
  • K231457 — SPARK Scan (August 18, 2023)
  • K221963 — Cumulus Functional Neurophysiology Platform (April 27, 2023)
  • K230073 — Okti (February 9, 2023)
  • K223644 — Neuronaute with IceCap 2 & IceCap 2 Small (January 12, 2023)
  • K220056 — iSyncWave (August 10, 2022)

FDA data resources