meddevicedb.com FDA Device Reference

OTSC Proctology

K150067 Class II Traditional
Decision Date
2015-09-16
Sponsor / Applicant
Ovesco Endoscopy AG

Technical Specification

510(k) Submission ID K150067
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2015-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OTSC Proctology received FDA 510(k) clearance under submission number K150067, sponsored by Ovesco Endoscopy AG. 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 2015-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.