meddevicedb.com FDA Device Reference

VSCORE WITH EKG SIGNAL GATING

K001682 Class II Traditional
Decision Date
2000-06-30
Sponsor / Applicant
Vital Images, Inc.

Technical Specification

510(k) Submission ID K001682
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2000-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VSCORE WITH EKG SIGNAL GATING received FDA 510(k) clearance under submission number K001682, sponsored by Vital Images, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-06-30.

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.