meddevicedb.com FDA Device Reference

FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES

K091490 Class II Special
Decision Date
2009-06-11
Sponsor / Applicant
Thd Spa

Technical Specification

510(k) Submission ID K091490
Product Code FER
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2009-06-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES received FDA 510(k) clearance under submission number K091490, 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 2009-06-11.

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.