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MODIFIED SONAMET BODY COMPOSITION ANALYZER

K032610 Class II Abbreviated
Decision Date
2004-03-01
Sponsor / Applicant
Life Measurement, Inc.

Technical Specification

510(k) Submission ID K032610
Product Code OAC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2004-03-01
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED SONAMET BODY COMPOSITION ANALYZER received FDA 510(k) clearance under submission number K032610, sponsored by Life Measurement, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-03-01.

Classification & Regulation

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