meddevicedb.com FDA Device Reference

MODIFICATION TO: ECAT LSO PET/CT SCANNER

K013504 Class II Special
Decision Date
2001-10-31
Sponsor / Applicant
Cti Pet Systems, Inc.

Technical Specification

510(k) Submission ID K013504
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2001-10-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: ECAT LSO PET/CT SCANNER received FDA 510(k) clearance under submission number K013504, sponsored by Cti Pet Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.