meddevicedb.com FDA Device Reference

Biograph mCT and mCT Flow PET/CT Scanners

K151486 Class II Special
Decision Date
2015-07-17
Sponsor / Applicant
Siemens Medical Solutions USA, Inc.

Technical Specification

510(k) Submission ID K151486
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2015-07-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Biograph mCT and mCT Flow PET/CT Scanners received FDA 510(k) clearance under submission number K151486, sponsored by Siemens Medical Solutions USA, 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 2015-07-17.

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.