meddevicedb.com FDA Device Reference

QUALITY REPORTS

K142142 Class II Traditional
Decision Date
2014-12-05
Sponsor / Applicant
Sun Nuclear Corporation

Technical Specification

510(k) Submission ID K142142
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2014-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUALITY REPORTS received FDA 510(k) clearance under submission number K142142, sponsored by Sun Nuclear Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.