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EG-3830UT, VIDEO ULTRASOUND GASTROSCOPE

K031789 Class II Traditional
Decision Date
2003-08-08
Sponsor / Applicant
Pentax Precision Instrument Corp.

Technical Specification

510(k) Submission ID K031789
Product Code ODG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2003-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EG-3830UT, VIDEO ULTRASOUND GASTROSCOPE received FDA 510(k) clearance under submission number K031789, sponsored by Pentax Precision Instrument Corp.. 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 2003-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code ODG and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.