BODYLOG ENHANCED STRESS REDUCTION PACKAGE— 510(k) K902450

Name: FDA 510(k) clearance K902450
Creator: U.S. Food and Drug Administration
Published: 1991-01-25

Substantially Equivalent

Bodylog, Inc.

FDA 510(k) clearance K902450 for BODYLOG ENHANCED STRESS REDUCTION PACKAGE, Substantially Equivalent on 1991-01-25. Applicant: Bodylog, Inc.. Device class: 2.

Clearance details

Applicant: Bodylog, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1990-06-01
Decision date: 1991-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.