BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230— 510(k) K062603

Name: FDA 510(k) clearance K062603
Creator: U.S. Food and Drug Administration
Published: 2007-02-15

Substantially Equivalent

Biospace Corporation Limited

FDA 510(k) clearance K062603 for BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230, Substantially Equivalent on 2007-02-15. Applicant: Biospace Corporation Limited. Device class: 2.

Clearance details

Applicant: Biospace Corporation Limited
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2006-09-01
Decision date: 2007-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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