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CAAS WORKSTATION

K133993 Class II Traditional
Decision Date
2014-03-25
Sponsor / Applicant
Pie Medical Imaging

Technical Specification

510(k) Submission ID K133993
Product Code IZI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1600
Decision Date 2014-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAAS WORKSTATION received FDA 510(k) clearance under submission number K133993, sponsored by Pie Medical Imaging. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-03-25.

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.