meddevicedb.com FDA Device Reference

3D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING

K002807 Class II Traditional
Decision Date
2000-12-01
Sponsor / Applicant
Acuson Corp.

Technical Specification

510(k) Submission ID K002807
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2000-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3D ORGAN ASSESSMENT W/ MAGNETIC POSITION SENSING received FDA 510(k) clearance under submission number K002807, sponsored by Acuson Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-12-01.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.