FDA 510(k) Application Details - K960047

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K960047
Device Name	Syringe, Piston
Applicant	JAMES K. BRANNON 5729 CANTERBURY DR. CULVER CITY, CA 90230-6547 US Other 510(k) Applications for this Company
Contact	JAMES K BRANNON Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/02/1996
Decision Date	05/24/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review