meddevicedb.com FDA Device Reference

CSMC CARDIAC SUITE- NUCLEAR MEDICINE SOFTWARE

K112474 Class II Special
Decision Date
2011-09-23
Sponsor / Applicant
Cedars-Sinai Medical Center

Technical Specification

510(k) Submission ID K112474
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2011-09-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CSMC CARDIAC SUITE- NUCLEAR MEDICINE SOFTWARE received FDA 510(k) clearance under submission number K112474, sponsored by Cedars-Sinai Medical Center. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-09-23.

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.