meddevicedb.com FDA Device Reference

UNIPOLAR OPTICAL BIOPSY FORCEPS

K983811 Class II Traditional
Decision Date
1998-12-24
Sponsor / Applicant
Olympus Winter & Ibe GmbH

Technical Specification

510(k) Submission ID K983811
Product Code KGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 1998-12-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIPOLAR OPTICAL BIOPSY FORCEPS received FDA 510(k) clearance under submission number K983811, sponsored by Olympus Winter & Ibe GmbH. 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 1998-12-24.

Classification & Regulation

This clearance is catalogued under FDA product code KGE and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.