FDA 510(k) Application Details - K230175

Device Classification Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)   More FDA Info for this Device
510(K) Number	K230175
Device Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)
Applicant	Canon Inc. 9-1 Imaikami-cho Nakahara-ku Kawasaki 211-8501 JP Other 510(k) Applications for this Company
Contact	Akira Hirai 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	01/20/2023
Decision Date	02/15/2023
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