meddevicedb.com FDA Device Reference

SIGNA PET/MR

K142098 Class II Traditional
Decision Date
2014-11-24
Sponsor / Applicant
Ge Medical Systems, LLC

Technical Specification

510(k) Submission ID K142098
Product Code OUO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2014-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIGNA PET/MR received FDA 510(k) clearance under submission number K142098, sponsored by Ge Medical Systems, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-11-24.

Classification & Regulation

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