FDA 510(k) Application Details - K012060

Device Classification Name	Scaler, Ultrasonic   More FDA Info for this Device
510(K) Number	K012060
Device Name	Scaler, Ultrasonic
Applicant	HU-FRIEDY MFG. CO.,INC. 3232 NORTH ROCKWELL ST. CHICAGO, IL 60618 US Other 510(k) Applications for this Company
Contact	KEITH DUNN 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	07/02/2001
Decision Date	07/27/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review