FDA 510(k) Application Details - K020431

Device Classification Name	Post, Root Canal   More FDA Info for this Device
510(K) Number	K020431
Device Name	Post, Root Canal
Applicant	EST. ANTHOGYR 164 RUE DES TROIS LACS SALLANCHES 74700 FR Other 510(k) Applications for this Company
Contact	CLAUDE ANTHOINE Other 510(k) Applications for this Contact
Regulation Number	872.3810   More FDA Info for this Regulation Number
Classification Product Code	ELR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2002
Decision Date	07/03/2002
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