meddevicedb.com FDA Device Reference

B6

K163429 Class II Traditional
Decision Date
2017-01-04
Sponsor / Applicant
Beijing East Whale Imaging Technology Co., Ltd.

Technical Specification

510(k) Submission ID K163429
Product Code OXO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2017-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

B6 received FDA 510(k) clearance under submission number K163429, sponsored by Beijing East Whale Imaging Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.