meddevicedb.com FDA Device Reference

CEDARS-SINAI QUANTITATIVE TI-201 ANALYSIS CTQ 2.0

K905222 Class II Traditional
Decision Date
1990-12-26
Sponsor / Applicant
Nuccardiac Software, Inc.

Technical Specification

510(k) Submission ID K905222
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 1990-12-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CEDARS-SINAI QUANTITATIVE TI-201 ANALYSIS CTQ 2.0 received FDA 510(k) clearance under submission number K905222, sponsored by Nuccardiac Software, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-12-26.

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.