THE EQUALIZER— 510(k) K915369

Name: FDA 510(k) clearance K915369
Creator: U.S. Food and Drug Administration
Published: 1993-03-22

Substantially Equivalent

Advanced Rehabilitative Technology, Inc.

FDA 510(k) clearance K915369 for THE EQUALIZER, Substantially Equivalent on 1993-03-22. Applicant: Advanced Rehabilitative Technology, Inc.. Device class: 1.

Clearance details

Applicant: Advanced Rehabilitative Technology, Inc.
Product code: Code IKE
Device class: Class 1
Regulation: 21 CFR 890.1615
Advisory panel: Physical Medicine
Date received: 1991-11-27
Decision date: 1993-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

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