FDA 510(k) Application Details - K190300

Device Classification Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)   More FDA Info for this Device
510(K) Number	K190300
Device Name	Solid State X-Ray Imager (Flat Panel/Digital Imager)
Applicant	Biokinemetrics Inc. 211 East 4th Street Carroll, IA 51401 US Other 510(k) Applications for this Company
Contact	Steven Kraus 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	02/12/2019
Decision Date	03/13/2019
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