FDA 510(k) Application Details - K223842

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K223842
Device Name	System, X-Ray, Stationary
Applicant	Carestream Health, Inc. Building 7, No. 1510 Chuanqiao Road China (Shanghai) Pilot Free Trade Zone 201206 CN Other 510(k) Applications for this Company
Contact	Jessica DeRyke 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	12/22/2022
Decision Date	01/20/2023
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