TRANSTEK GLASS BODY FAT ANALYZER
K-Number: K123781 · 2013-01-09
Advertisement
Device Summary
Frequently Asked Questions
What is the TRANSTEK GLASS BODY FAT ANALYZER?
TRANSTEK GLASS BODY FAT ANALYZER is a medical device that received FDA 510(k) clearance on 2013-01-09. The listed applicant is Zhongshan Transtek Electronics Co., Ltd.. The 510(k) number is K123781.
When did TRANSTEK GLASS BODY FAT ANALYZER receive FDA 510(k) clearance?
TRANSTEK GLASS BODY FAT ANALYZER received FDA 510(k) clearance on 2013-01-09, under 510(k) number K123781.
Who is the listed applicant for TRANSTEK GLASS BODY FAT ANALYZER?
The FDA 510(k) record lists Zhongshan Transtek Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSTEK GLASS BODY FAT ANALYZER?
The FDA product code for TRANSTEK GLASS BODY FAT ANALYZER is MNW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Zhongshan Transtek Electronics Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MNW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement