FDA 510(k) Application Details - DEN990002

Device Classification Name	Laser,Fluorescence Caries Detection   More FDA Info for this Device
510(K) Number	DEN990002
Device Name	Laser,Fluorescence Caries Detection
Applicant	KAVO AMERICA 340 EAST MAIN ST. LAKE ZURICH, IL 60047 US Other 510(k) Applications for this Company
Contact	DOUGLAS COCHRANE Other 510(k) Applications for this Contact
Regulation Number	872.1745   More FDA Info for this Regulation Number
Classification Product Code	NBL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/12/1999
Decision Date	02/22/2000
Decision	DENG -
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review