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REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS

K022751 Class II Traditional
Decision Date
2002-11-04
Sponsor / Applicant
Medical Device Services

Technical Specification

510(k) Submission ID K022751
Product Code KGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 2002-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS received FDA 510(k) clearance under submission number K022751, sponsored by Medical Device Services. 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 2002-11-04.

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.