FDA 510(k) Application Details - K023323

Device Classification Name	Syringe, Antistick   More FDA Info for this Device
510(K) Number	K023323
Device Name	Syringe, Antistick
Applicant	FUTURA MEDICAL TECHNOLOGY 380 STEVENS AVE., SUITE 212 SOLANA BEACH, CA 92075 US Other 510(k) Applications for this Company
Contact	DAVID OLMSTEAD Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	MEG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/04/2002
Decision Date	10/29/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review