FDA 510(k) Application Details - K213637

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K213637
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	Jazz Imaging LLC dba JAZZ Imaging San Jose, CA 95131 US Other 510(k) Applications for this Company
Contact	Todd C Miller Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	MUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/18/2021
Decision Date	12/10/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review