THE MIRAGE SYSTEM BIOFEEDBACK INTERFACE— 510(k) K941938

Name: FDA 510(k) clearance K941938
Creator: U.S. Food and Drug Administration
Published: 1994-08-05

Substantially Equivalent

Intercare Diagnostics, Inc.

FDA 510(k) clearance K941938 for THE MIRAGE SYSTEM BIOFEEDBACK INTERFACE, Substantially Equivalent on 1994-08-05. Applicant: Intercare Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Intercare Diagnostics, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1994-04-21
Decision date: 1994-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Inglewood, CA, US

Download summary PDF View on FDA.gov ↗

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