TRANSTEK GLASS BODY FAT ANALYZER— 510(k) K123781

Name: FDA 510(k) clearance K123781
Creator: U.S. Food and Drug Administration
Published: 2013-01-09

Substantially Equivalent

Zhongshan Transtek Electronics Co., Ltd.

FDA 510(k) clearance K123781 for TRANSTEK GLASS BODY FAT ANALYZER, Substantially Equivalent on 2013-01-09. Applicant: Zhongshan Transtek Electronics Co., Ltd.. Device class: 2.

Clearance details

Applicant: Zhongshan Transtek Electronics Co., Ltd.
Product code: Code MNW
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2012-12-10
Decision date: 2013-01-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Chengdu, Sichuan, CN

Download summary PDF View on FDA.gov ↗

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