meddevicedb.com FDA Device Reference

APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE

K012951 Class II Traditional
Decision Date
2001-11-09
Sponsor / Applicant
Circon Video

Technical Specification

510(k) Submission ID K012951
Product Code FGB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2001-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE received FDA 510(k) clearance under submission number K012951, sponsored by Circon Video. 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 2001-11-09.

Classification & Regulation

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