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DISPOSABLE BIOPSY FORCEP FOR FLEXIBLE ENDOSCOPES

K902066 Class II Traditional
Decision Date
1990-09-06
Sponsor / Applicant
Endo-Scientific, Inc.

Technical Specification

510(k) Submission ID K902066
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1990-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE BIOPSY FORCEP FOR FLEXIBLE ENDOSCOPES received FDA 510(k) clearance under submission number K902066, sponsored by Endo-Scientific, 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 1990-09-06.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.