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510(k) K904763

MENTOR EEG SYSTEM by Oxford Medilog, Inc. — Product Code GWQ

K904763 is an FDA 510(k) premarket notification submitted by Oxford Medilog, Inc. for the device "MENTOR EEG SYSTEM". The FDA issued a decision of Substantially Equivalent on April 10, 1991. The device falls under product code GWQ (Full-Montage Standard Electroencephalograph), a Class II device regulated under 21 CFR 882.1400. Oxford Medilog, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 10, 1991
Date Received
October 22, 1990
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 Oxford Medilog, Inc.

  • K923737 — MODEL MEDILOG RAPIDE (January 5, 1994)
  • K920295 — MEDILOG EXCEL ECG ANALYSIS SYSTEM (MODIFIED) (August 18, 1992)
  • K912890 — MODEL SONICAID AXIS (January 9, 1992)
  • K912639 — SONICAID TEAM (December 31, 1991)
  • K902690 — SONICAID MODEL MERIDIAN 800 (February 5, 1991)
  • K895909 — SONICAID MODEL VASOFLO 4 (July 9, 1990)
  • K896535 — MEDILOG OPTIMA (January 18, 1990)
  • K891383 — MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM (June 1, 1989)
  • K890330 — MEDILOG 6000-FD REPORT GENERATOR (April 20, 1989)
  • K890338 — MEDILOG EDITOR (April 19, 1989)

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