FDA 510(k) Application Details - K961275

Device Classification Name	Handpiece, Air-Powered, Dental   More FDA Info for this Device
510(K) Number	K961275
Device Name	Handpiece, Air-Powered, Dental
Applicant	MICRO-MEGA SOCIETE ANONYME 5-12 RUE DU TUNNEL CEDEX BESANCON 25006 FR Other 510(k) Applications for this Company
Contact	JIM BADOZ Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EFB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/03/1996
Decision Date	01/17/1997
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