FDA 510(k) Application Details - K033345

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K033345
Device Name	System, X-Ray, Stationary
Applicant	ANALOGIC CORP. 8 CENTENNIAL DR. PEABODY, MA 01960 US Other 510(k) Applications for this Company
Contact	MARVIN ROSENBAUM Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/20/2003
Decision Date	11/19/2003
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