MICROELECTROENCEPHALOGRAPHY PROFESSIONAL SYSTEM 5000 (EEG PRO SYSTEM 5000)— 510(k) K991077

Name: FDA 510(k) clearance K991077
Creator: U.S. Food and Drug Administration
Published: 1999-06-09

Substantially Equivalent

Microrecording Systems Consultants, LLC

FDA 510(k) clearance K991077 for MICROELECTROENCEPHALOGRAPHY PROFESSIONAL SYSTEM 5000 (EEG PRO SYSTEM 5000), Substantially Equivalent on 1999-06-09. Applicant: Microrecording Systems Consultants, LLC. Device class: 2.

Clearance details

Applicant: Microrecording Systems Consultants, LLC
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 1999-03-31
Decision date: 1999-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pasadena, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZL

view all

K253970 — Wovyn Depth Electrode2026-04-17
K250363 — Depth Electrode (17+ models)2025-11-05
K250601 — Neuro Omega System; NeuroSmart System2025-03-30
K223269 — Spencer Probe Depth Electrodes2023-05-18
K223276 — Anchor Bolts as Accessories to Depth Electrodes2023-05-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.