meddevicedb.com FDA Device Reference

Brush Biopsy Set ; Deflectable Brush Biopsy Set

K182231 Class II Traditional
Decision Date
2019-05-01
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K182231
Product Code FDX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2019-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Brush Biopsy Set ; Deflectable Brush Biopsy Set received FDA 510(k) clearance under submission number K182231, sponsored by Cook Incorporated. 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 2019-05-01.

Classification & Regulation

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