meddevicedb.com FDA Device Reference

GE ADVANCE NXI PET SYSTEM

K003849 Class II Special
Decision Date
2000-12-22
Sponsor / Applicant
Ge Medical Systems, Inc.

Technical Specification

510(k) Submission ID K003849
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2000-12-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GE ADVANCE NXI PET SYSTEM received FDA 510(k) clearance under submission number K003849, sponsored by Ge Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.