RELIEFBAND— 510(k) K980333

Substantially Equivalent

Woodside Biomedical, Inc.

FDA 510(k) clearance K980333 for RELIEFBAND, Substantially Equivalent on 1998-02-18. 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: 1998-01-28
Decision date: 1998-02-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Woodside Biomedical, Inc.

K020180 — RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL2002-03-21
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Data sourced from openFDA. This site is unofficial and independent of the FDA.