meddevicedb.com FDA Device Reference

1.5T PEDIATRIC HEAD AND SPINE ARRAY MODEL

K060689 Class II Special
Decision Date
2006-03-31
Sponsor / Applicant
Resonance Innovations, LLC

Technical Specification

510(k) Submission ID K060689
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2006-03-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1.5T PEDIATRIC HEAD AND SPINE ARRAY MODEL received FDA 510(k) clearance under submission number K060689, sponsored by Resonance Innovations, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.