FDA 510(k) Application Details - K091928

Device Classification Name	Cabinet,X-Ray System   More FDA Info for this Device
510(K) Number	K091928
Device Name	Cabinet,X-Ray System
Applicant	BIOPTICS, INC. 3440 E BRITANNIA DR SUITE 150 TUCSON, AZ 85743 US Other 510(k) Applications for this Company
Contact	AKIF BAYSAL Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	MWP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/30/2009
Decision Date	06/16/2010
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