FDA 510(k) Application Details - K082432

Device Classification Name	Cabinet,X-Ray System   More FDA Info for this Device
510(K) Number	K082432
Device Name	Cabinet,X-Ray System
Applicant	BIOPTICS, INC. 15546 W. GELDING DR. SURPRISE, AZ 85379 US Other 510(k) Applications for this Company
Contact	PATRICIA WADE 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	08/22/2008
Decision Date	11/21/2008
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