meddevicedb.com FDA Device Reference

MRI MARKER

K131689 Class II Traditional
Decision Date
2013-11-20
Sponsor / Applicant
C4 Imaging, LLC

Technical Specification

510(k) Submission ID K131689
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2013-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MRI MARKER received FDA 510(k) clearance under submission number K131689, sponsored by C4 Imaging, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2013-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.