meddevicedb.com FDA Device Reference

UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000

K884836 Class II Traditional
Decision Date
1988-12-06
Sponsor / Applicant
Meditron Devices, Inc.

Technical Specification

510(k) Submission ID K884836
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1988-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000 received FDA 510(k) clearance under submission number K884836, sponsored by Meditron Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1988-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.