FDA 510(k) Application Details - K041279

Device Classification Name	Handpiece, Direct Drive, Ac-Powered   More FDA Info for this Device
510(K) Number	K041279
Device Name	Handpiece, Direct Drive, Ac-Powered
Applicant	ANTHOGYR 164 RUE DE TROIS LACS SALLANCHES 74700 FR Other 510(k) Applications for this Company
Contact	ERIC GENEVE 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	05/13/2004
Decision Date	09/23/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review