meddevicedb.com FDA Device Reference

MULTIPLE PRIVATE LABEL

K100162 Class I Traditional
Decision Date
2010-03-24
Sponsor / Applicant
Biogreen Yields Sdn.Bhd

Technical Specification

510(k) Submission ID K100162
Product Code LZA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 2010-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIPLE PRIVATE LABEL received FDA 510(k) clearance under submission number K100162, sponsored by Biogreen Yields Sdn.Bhd. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2010-03-24.

Classification & Regulation

This clearance is catalogued under FDA product code LZA and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.