meddevicedb.com FDA Device Reference

MMG BILE BAG

K911129 Class II Traditional
Decision Date
1991-08-07
Sponsor / Applicant
Medical Technologies of Georgia

Technical Specification

510(k) Submission ID K911129
Product Code EXF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 1991-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MMG BILE BAG received FDA 510(k) clearance under submission number K911129, sponsored by Medical Technologies of Georgia. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1991-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code EXF and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.