FDA 510(k) Application Details - K992819

Device Classification Name	Syringe, Cartridge   More FDA Info for this Device
510(K) Number	K992819
Device Name	Syringe, Cartridge
Applicant	SPINTECH, INC. 2000 M. ST. NW # 700 WASHINGTON, DC 20036 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	08/20/1999
Decision Date	05/11/2000
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