DUTECK BODY COMPOSITION ANALYZER— 510(k) K060642

Name: FDA 510(k) clearance K060642
Creator: U.S. Food and Drug Administration
Published: 2006-06-07

Substantially Equivalent

Duteck Industrial Co., Ltd.

FDA 510(k) clearance K060642 for DUTECK BODY COMPOSITION ANALYZER, Substantially Equivalent on 2006-06-07. Applicant: Duteck Industrial Co., Ltd.. Device class: 2.

Clearance details

Applicant: Duteck Industrial Co., Ltd.
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2006-03-10
Decision date: 2006-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, TW

Download summary PDF View on FDA.gov ↗

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