INNERSCAN BODY COMPOSITION MONITOR, INNERSCAN SEGMENTAL BODY COMPOSITION MONITOR— 510(k) K062652

Name: FDA 510(k) clearance K062652
Creator: U.S. Food and Drug Administration
Published: 2006-12-28

Substantially Equivalent

Tanita Corporation of America

FDA 510(k) clearance K062652 for INNERSCAN BODY COMPOSITION MONITOR, INNERSCAN SEGMENTAL BODY COMPOSITION MONITOR, Substantially Equivalent on 2006-12-28. Applicant: Tanita Corporation of America. Device class: 2.

Clearance details

Applicant: Tanita Corporation of America
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2006-09-07
Decision date: 2006-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington Heights, IL, US

Download summary PDF View on FDA.gov ↗

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