FDA 510(k) Application Details - K960665

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K960665
Device Name	System, Image Processing, Radiological
Applicant	CONE INSTRUMENTS, INC. 5201 NAIMAN PKWY. SOLON, OH 44139 US Other 510(k) Applications for this Company
Contact	JAY C CONE Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/20/1996
Decision Date	05/07/1996
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