FDA 510(k) Application Details - K991680

Device Classification Name	Introducer, Syringe Needle   More FDA Info for this Device
510(K) Number	K991680
Device Name	Introducer, Syringe Needle
Applicant	ANDROSYSTEMS SRL VIALE LIEGI, 12 ROME 00198 IT Other 510(k) Applications for this Company
Contact	ERMANNO GRECO Other 510(k) Applications for this Contact
Regulation Number	880.6920   More FDA Info for this Regulation Number
Classification Product Code	KZH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/17/1999
Decision Date	06/03/1999
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