FDA 510(k) Application Details - K990511

Device Classification Name	Needle, Dental   More FDA Info for this Device
510(K) Number	K990511
Device Name	Needle, Dental
Applicant	SCHIFF & CO. 1129 BLOOMFIELD AVE. WEST CALDWELL, NJ 07006 US Other 510(k) Applications for this Company
Contact	ROBERT SCHIFF Other 510(k) Applications for this Contact
Regulation Number	872.4730   More FDA Info for this Regulation Number
Classification Product Code	DZM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/18/1999
Decision Date	04/27/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review