meddevicedb.com FDA Device Reference

CS IMAGING

K113419 Class II Traditional
Decision Date
2012-02-16
Sponsor / Applicant
Trophy

Technical Specification

510(k) Submission ID K113419
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2012-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CS IMAGING received FDA 510(k) clearance under submission number K113419, sponsored by Trophy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.