meddevicedb.com FDA Device Reference

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0

K203717 Class II Traditional
Decision Date
2021-06-30
Sponsor / Applicant
Fujifilm Corporaton

Technical Specification

510(k) Submission ID K203717
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2021-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 received FDA 510(k) clearance under submission number K203717, sponsored by Fujifilm Corporaton. 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 2021-06-30.

Classification & Regulation

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