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FDA 510(k)

AQ-830 SLIM BODY, BODY FAT MONITOR

K-Number: K052678 · 2005-12-27

ApplicantLimax Electronics Co., Ltd.
Decision Date2005-12-27
Product CodeMNW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AQ-830 SLIM BODY, BODY FAT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Limax Electronics Co., Ltd.. It received FDA 510(k) clearance on 2005-12-27 under 510(k) number K052678. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQ-830 SLIM BODY, BODY FAT MONITOR?

AQ-830 SLIM BODY, BODY FAT MONITOR is a medical device that received FDA 510(k) clearance on 2005-12-27. The listed applicant is Limax Electronics Co., Ltd.. The 510(k) number is K052678.

When did AQ-830 SLIM BODY, BODY FAT MONITOR receive FDA 510(k) clearance?

AQ-830 SLIM BODY, BODY FAT MONITOR received FDA 510(k) clearance on 2005-12-27, under 510(k) number K052678.

Who is the listed applicant for AQ-830 SLIM BODY, BODY FAT MONITOR?

The FDA 510(k) record lists Limax Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQ-830 SLIM BODY, BODY FAT MONITOR?

The FDA product code for AQ-830 SLIM BODY, BODY FAT MONITOR is MNW.

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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.

K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.K130856BIA / VITALITY ANALYZERIpgdx, LLCK130777INBODYBiospace Corporation LimitedK130952PRECISION ONE LIFECARE; DETECTO; DETECTOPrecision One Lifecare, Ltd.K131394TRANSTEK GLASS BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.K130311TRANSTEK BODY FAT ANALYZERGuangdong Transtek Medical Electronics Co., Ltd.

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.

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