meddevicedb.com FDA Device Reference

COLOSHIELD COLONOSCOPY DRAPE MODEL E2000

K020581 Class II Traditional
Decision Date
2002-09-18
Sponsor / Applicant
Medical Concepts Development, Inc.

Technical Specification

510(k) Submission ID K020581
Product Code KKX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2002-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COLOSHIELD COLONOSCOPY DRAPE MODEL E2000 received FDA 510(k) clearance under submission number K020581, sponsored by Medical Concepts Development, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2002-09-18.

Classification & Regulation

This clearance is catalogued under FDA product code KKX and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.