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GE DISCOVERY IGS ANGIOGRAPHIC,FLUOROSCOPIC X-RAY SYSTEM

K113403 Class II Traditional
Decision Date
2012-02-14
Sponsor / Applicant
GE Medical Systems SCS

Technical Specification

510(k) Submission ID K113403
Product Code OWB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2012-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GE DISCOVERY IGS ANGIOGRAPHIC,FLUOROSCOPIC X-RAY SYSTEM received FDA 510(k) clearance under submission number K113403, sponsored by GE Medical Systems SCS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code OWB and 21 CFR 892.1650, within the Radiology review panel as a Class II device.