FDA 510(k) Application Details - K983430

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K983430
Device Name	Syringe, Piston
Applicant	MEDICORE, INC. 2647 WEST 81 ST. HIALEAH, FL 33016 US Other 510(k) Applications for this Company
Contact	BONNIE J KAPLAN 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	09/29/1998
Decision Date	02/09/1999
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