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WI-FI BODY SCALE

K120896 Class II Traditional
Decision Date
2012-07-26
Sponsor / Applicant
Andon Health Co, Ltd.

Technical Specification

510(k) Submission ID K120896
Product Code MNW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2012-07-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WI-FI BODY SCALE received FDA 510(k) clearance under submission number K120896, sponsored by Andon Health 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 2012-07-26.

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.