FDA 510(k) Application Details - K960920

Device Classification Name	More FDA Info for this Device
510(K) Number	K960920
Device Name	CLINIX MP
Applicant	PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. HIGHLAND HEIGHTS, OH 44143 US Other 510(k) Applications for this Company
Contact	ROBERT L TUROCY Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/06/1996
Decision Date	05/20/1996
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