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ATLAS MULTI-PURPOSE DSA SYSTEM

K010391 Class II Traditional
Decision Date
2001-03-12
Sponsor / Applicant
Cares Built, Inc.

Technical Specification

510(k) Submission ID K010391
Product Code IZI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1600
Decision Date 2001-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATLAS MULTI-PURPOSE DSA SYSTEM received FDA 510(k) clearance under submission number K010391, sponsored by Cares Built, 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 2001-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code IZI and 21 CFR 892.1600, within the Radiology review panel as a Class II device.