THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS— 510(k) K854208

Name: FDA 510(k) clearance K854208
Creator: U.S. Food and Drug Administration
Published: 1986-01-14

Substantially Equivalent

Bodylog, Inc.

FDA 510(k) clearance K854208 for THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS, Substantially Equivalent on 1986-01-14. 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: 1985-10-17
Decision date: 1986-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Kisco, NY, 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.