RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R— 510(k) K983907

Name: FDA 510(k) clearance K983907
Creator: U.S. Food and Drug Administration
Published: 1999-12-09

Substantially Equivalent

Woodside Biomedical, Inc.

FDA 510(k) clearance K983907 for RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R, Substantially Equivalent on 1999-12-09. 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: 1998-11-03
Decision date: 1999-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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