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INHEALTH SOFT SLEEVE COLONOSCOPE SPLINT, MODEL CS1200

K023259 Class II Traditional
Decision Date
2002-12-26
Sponsor / Applicant
Helix Medical, Inc.

Technical Specification

510(k) Submission ID K023259
Product Code FDF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INHEALTH SOFT SLEEVE COLONOSCOPE SPLINT, MODEL CS1200 received FDA 510(k) clearance under submission number K023259, sponsored by Helix Medical, 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 2002-12-26.

Classification & Regulation

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