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AVITA BF1 (VITALIO) BODY FAT ANALYZER

K020738 Class II Traditional
Decision Date
2003-05-22
Sponsor / Applicant
Avita Corporation

Technical Specification

510(k) Submission ID K020738
Product Code MNW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2003-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AVITA BF1 (VITALIO) BODY FAT ANALYZER received FDA 510(k) clearance under submission number K020738, sponsored by Avita Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-05-22.

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.