FDA 510(k) Application Details - K012505

Device Classification Name	Unit, Operative Dental   More FDA Info for this Device
510(K) Number	K012505
Device Name	Unit, Operative Dental
Applicant	SOPRO PLACE ST. CHRISTOPHE LES ACCATES-LA VALENTINE MARSEILLE F-13011 FR Other 510(k) Applications for this Company
Contact	PIERRE MONTILLOT Other 510(k) Applications for this Contact
Regulation Number	872.6640   More FDA Info for this Regulation Number
Classification Product Code	EIA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/03/2001
Decision Date	10/05/2001
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