meddevicedb.com FDA Device Reference

BARS Set (100.60)

K241858 Class II Traditional
Decision Date
2024-08-26
Sponsor / Applicant
Ovesco Endoscopy AG

Technical Specification

510(k) Submission ID K241858
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2024-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARS Set (100.60) received FDA 510(k) clearance under submission number K241858, 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 2024-08-26.

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.