RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL— 510(k) K020180

Name: FDA 510(k) clearance K020180
Creator: U.S. Food and Drug Administration
Published: 2002-03-21

Substantially Equivalent

Woodside Biomedical, Inc.

FDA 510(k) clearance K020180 for RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL, Substantially Equivalent on 2002-03-21. Applicant: Woodside Biomedical, Inc.. Device class: 2.

Clearance details

Applicant: Woodside Biomedical, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2002-01-18
Decision date: 2002-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, CA, US

Download summary PDF View on FDA.gov ↗

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