FDA 510(k) Application Details - K081191

Device Classification Name	Handpiece, Direct Drive, Ac-Powered   More FDA Info for this Device
510(K) Number	K081191
Device Name	Handpiece, Direct Drive, Ac-Powered
Applicant	NOUVAG AG REUSSWEHRSTRASSE 1 GEBENSTORF CH-5412 CH Other 510(k) Applications for this Company
Contact	ERICH FORSTER Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EKX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/28/2008
Decision Date	08/07/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review