meddevicedb.com FDA Device Reference

THD N-ANO ANOSCOPE

K133687 Class II Special
Decision Date
2013-12-11
Sponsor / Applicant
Thd Spa

Technical Specification

510(k) Submission ID K133687
Product Code FER
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2013-12-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THD N-ANO ANOSCOPE received FDA 510(k) clearance under submission number K133687, sponsored by Thd Spa. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2013-12-11.

Classification & Regulation

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