Transtek Body Fat Analyzer

FDA 510(k) K130311 · Guangdong Transtek Medical Electronics Co., Ltd.

Substantially Equivalent

510(k) numberK130311

Submission

Device name
Transtek Body Fat Analyzer
Applicant
Guangdong Transtek Medical Electronics Co., Ltd.
Chengdu, Sichuan, CN
Received
February 8, 2013
Decision date
May 30, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNW – Analyzer, Body Composition
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2770
Specialty
Cardiovascular

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Questions and answers

When was Transtek Body Fat Analyzer cleared by the FDA?

Transtek Body Fat Analyzer (K130311) received a 510(k) decision of Substantially Equivalent on May 30, 2013, 111 days after the submission was received.

What is the product code of K130311?

The FDA product code is MNW – Analyzer, Body Composition, a Class II (moderate risk) device regulated under 21 CFR 870.2770.