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FLEXIBLE FIBER OPTIC ENDOSCOPE

K922826 Class II Traditional
Decision Date
1993-02-19
Sponsor / Applicant
Optimed Technologies, Inc.

Technical Specification

510(k) Submission ID K922826
Product Code FGA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1993-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLEXIBLE FIBER OPTIC ENDOSCOPE received FDA 510(k) clearance under submission number K922826, sponsored by Optimed Technologies, Inc.. 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 1993-02-19.

Classification & Regulation

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