meddevicedb.com FDA Device Reference

BIOSPACE BODY COMPOSITION ANALYZER

K141483 Class II Traditional
Decision Date
2014-09-23
Sponsor / Applicant
Biospace Corporation Limited

Technical Specification

510(k) Submission ID K141483
Product Code MNW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2014-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSPACE BODY COMPOSITION ANALYZER received FDA 510(k) clearance under submission number K141483, sponsored by Biospace Corporation Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-09-23.

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.