meddevicedb.com FDA Device Reference

WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR

K103596 Class II Special
Decision Date
2011-03-29
Sponsor / Applicant
Fujifilm Medical Systems U.S.A, Inc.

Technical Specification

510(k) Submission ID K103596
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2011-03-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR received FDA 510(k) clearance under submission number K103596, sponsored by Fujifilm Medical Systems U.S.A, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.