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IMPEDIMED - BODY COMPOSITION ANALYZER, MODEL IMP SFB7

K052319 Class II Traditional
Decision Date
2006-04-04
Sponsor / Applicant
Impedimed Pty , Ltd.

Technical Specification

510(k) Submission ID K052319
Product Code MNW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2006-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPEDIMED - BODY COMPOSITION ANALYZER, MODEL IMP SFB7 received FDA 510(k) clearance under submission number K052319, sponsored by Impedimed Pty , 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 2006-04-04.

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.