FDA 510(k) Application Details - K991758

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K991758
Device Name	Syringe, Piston
Applicant	THE KENDAL CO. 15 HAMPSHIRE ST. MANSFIELD, MA 02048-1108 US Other 510(k) Applications for this Company
Contact	FRANK J FUCILE 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	05/24/1999
Decision Date	06/14/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review