FDA 510(k) Application Details - K161459

Device Classification Name Solid State X-Ray Imager (Flat Panel/Digital Imager)

  More FDA Info for this Device
510(K) Number K161459
Device Name Solid State X-Ray Imager (Flat Panel/Digital Imager)
Applicant VARIAN MEDICAL SYSTEMS, X-RAY PRODUCTS-INFIMED
121 METROPOLITAN DRIVE
LIVERPOOL, NY 13088 US
Other 510(k) Applications for this Company
Contact Catherine Mulcahy
Other 510(k) Applications for this Contact
Regulation Number 892.1650

  More FDA Info for this Regulation Number
Classification Product Code MQB
Other 510(k) Applications for this Device

  More FDA Info for this Product Code
Date Received 05/26/2016
Decision Date 09/06/2016
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact