FDA 510(k) Application Details - K001341

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K001341
Device Name	System, X-Ray, Stationary
Applicant	ANALOGIC CORP. 8 CENTENNIAL DR. PEABODY, MA 01960 US Other 510(k) Applications for this Company
Contact	ROBERT H FRENCH 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	04/27/2000
Decision Date	06/02/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review