meddevicedb.com FDA Device Reference

Stroke VCAR

K152584 Class II Traditional
Decision Date
2016-01-20
Sponsor / Applicant
GE Medical Systems SCS

Technical Specification

510(k) Submission ID K152584
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2016-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Stroke VCAR received FDA 510(k) clearance under submission number K152584, sponsored by GE Medical Systems SCS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-01-20.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.