meddevicedb.com FDA Device Reference

TRU-CABLE

K063309 Class II Traditional
Decision Date
2007-01-12
Sponsor / Applicant
Truphatek International, Ltd.

Technical Specification

510(k) Submission ID K063309
Product Code FFS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2007-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRU-CABLE received FDA 510(k) clearance under submission number K063309, sponsored by Truphatek International, Ltd.. 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 2007-01-12.

Classification & Regulation

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