FDA 510(k) Application Details - K213700

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K213700
Device Name	System, X-Ray, Stationary
Applicant	Siemens Medical Solutions USA, Inc. 40 Liberty Boulevard Malvern, PA 19355 US Other 510(k) Applications for this Company
Contact	Denise Adams Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/23/2021
Decision Date	12/13/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review