FDA 510(k) Application Details - K062702

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K062702
Device Name	Syringe, Piston
Applicant	ULTIMED, INC. 5353 WAYZATA BLVD. SUITE 505 MINNEAPOLIS, MN 55416-1334 US Other 510(k) Applications for this Company
Contact	CAROLE STAMP 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	09/11/2006
Decision Date	11/29/2006
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