meddevicedb.com FDA Device Reference

JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps Valve

K210625 Class II Traditional
Decision Date
2021-09-10
Sponsor / Applicant
Fujifilm Medwork GmbH

Technical Specification

510(k) Submission ID K210625
Product Code ODC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2021-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JAZZ Suction Valve, JAZZ Air/Water Valve, JAZZ Forceps Valve received FDA 510(k) clearance under submission number K210625, sponsored by Fujifilm Medwork GmbH. 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 2021-09-10.

Classification & Regulation

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