meddevicedb.com FDA Device Reference

vRad PACS with Mammography

K162145 Class II Abbreviated
Decision Date
2016-10-25
Sponsor / Applicant
Virtual Radiologic Corporation

Technical Specification

510(k) Submission ID K162145
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2016-10-25
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

vRad PACS with Mammography received FDA 510(k) clearance under submission number K162145, sponsored by Virtual Radiologic Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.