FDA 510(k) Application Details - K213713

Device Classification Name System, X-Ray, Tomography, Computed

  More FDA Info for this Device
510(K) Number K213713
Device Name System, X-Ray, Tomography, Computed
Applicant Siemens Healthcare GmBh
40 Liberty Blvd. Mail Code 65-1
Malvern, PA 19355 US
Other 510(k) Applications for this Company
Contact Lauren Bentley
Other 510(k) Applications for this Contact
Regulation Number 892.1750

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

  More FDA Info for this Product Code
Date Received 11/24/2021
Decision Date 08/11/2022
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