FDA 510(k) Application Details - K960248

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K960248
Device Name	Syringe, Piston
Applicant	PHYSICIAN INDUSTRIES, INC. 101 NORTH 700 WST P.O. BOX 540793 NORTH SALT LAKE, UT 84054-0793 US Other 510(k) Applications for this Company
Contact	BRIAN BAKER 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	01/16/1996
Decision Date	04/12/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review