FDA 510(k) Application Details - K964320

Device Classification Name	Scaler, Ultrasonic   More FDA Info for this Device
510(K) Number	K964320
Device Name	Scaler, Ultrasonic
Applicant	TONY RISO CO., INC. 17070 COLLINS AVENUE #263 MIAMI BEACH, FL 33160 US Other 510(k) Applications for this Company
Contact	CHARLES L VENTURI Other 510(k) Applications for this Contact
Regulation Number	872.4850   More FDA Info for this Regulation Number
Classification Product Code	ELC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/29/1996
Decision Date	01/23/1997
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