FDA 510(k) Application Details - K061904

Device Classification Name	Syringe, Cartridge   More FDA Info for this Device
510(K) Number	K061904
Device Name	Syringe, Cartridge
Applicant	MILESTONE SCIENTIFIC, INC. 5335 WISCONSIN AVE NW SUITE 440 WASHINGTON, DC 20015 US Other 510(k) Applications for this Company
Contact	DANIEL J MANELLI Other 510(k) Applications for this Contact
Regulation Number	872.6770   More FDA Info for this Regulation Number
Classification Product Code	EJI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/05/2006
Decision Date	08/08/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review