FDA 510(k) Application Details - K071430

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K071430
Device Name	System, X-Ray, Stationary
Applicant	ANALOGIC CORP. 8 CENTENNIAL DR. CENTENNIAL INDUSTRIAL PARK PEABODY, MA 01960 US Other 510(k) Applications for this Company
Contact	DONALD J SHERRATT 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	05/23/2007
Decision Date	06/21/2007
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