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STARSPEED SERIES CT SCANNER SYSTEMS

K052855 Class II Traditional
Decision Date
2005-10-28
Sponsor / Applicant
GE Healthcare

Technical Specification

510(k) Submission ID K052855
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 2005-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STARSPEED SERIES CT SCANNER SYSTEMS received FDA 510(k) clearance under submission number K052855, sponsored by GE Healthcare. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-10-28.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.