FDA 510(k) Application Details - K962017

Device Classification Name	Injector, Jet, Mechanical-Powered   More FDA Info for this Device
510(K) Number	K962017
Device Name	Injector, Jet, Mechanical-Powered
Applicant	AMERICAN JET INJECTOR CORP. 880 ORCHARD LN. LANSDALE, PA 19446-4520 US Other 510(k) Applications for this Company
Contact	ROBERT W HARRINGTON Other 510(k) Applications for this Contact
Regulation Number	872.4475   More FDA Info for this Regulation Number
Classification Product Code	EGM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/23/1996
Decision Date	07/26/1996
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