MEDRELIEF ST SERIES, MODELS RT-50, ST-100, ST 150, ST-200, ST-300— 510(k) K060669

Name: FDA 510(k) clearance K060669
Creator: U.S. Food and Drug Administration
Published: 2006-10-13

Substantially Equivalent

Healthonics, Inc.

FDA 510(k) clearance K060669 for MEDRELIEF ST SERIES, MODELS RT-50, ST-100, ST 150, ST-200, ST-300, Substantially Equivalent on 2006-10-13. Applicant: Healthonics, Inc.. Device class: 2.

Clearance details

Applicant: Healthonics, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2006-03-14
Decision date: 2006-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Ellenton, SC, US

Download summary PDF View on FDA.gov ↗

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