meddevicedb.com FDA Device Reference

LIFEGLOBAL PROTEIN SUPPLEMENT

K092578 Class II Traditional
Decision Date
2010-04-05
Sponsor / Applicant
Genx Intl., Inc.

Technical Specification

510(k) Submission ID K092578
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2010-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFEGLOBAL PROTEIN SUPPLEMENT received FDA 510(k) clearance under submission number K092578, sponsored by Genx Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2010-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.