meddevicedb.com FDA Device Reference

BSD4343R Digital Flat Panel X-ray Detector

K171485 Class II Special
Decision Date
2017-06-21
Sponsor / Applicant
Bontech, Inc.

Technical Specification

510(k) Submission ID K171485
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2017-06-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BSD4343R Digital Flat Panel X-ray Detector received FDA 510(k) clearance under submission number K171485, sponsored by Bontech, 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 2017-06-21.

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.