meddevicedb.com FDA Device Reference

AQ-830 SLIM BODY, BODY FAT MONITOR

K052678 Class II Traditional
Decision Date
2005-12-27
Sponsor / Applicant
Limax Electronics Co., Ltd.

Technical Specification

510(k) Submission ID K052678
Product Code MNW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2005-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQ-830 SLIM BODY, BODY FAT MONITOR received FDA 510(k) clearance under submission number K052678, sponsored by Limax Electronics Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code MNW and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.