FDA 510(k) Application Details - K032773

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K032773
Device Name	Resin, Denture, Relining, Repairing, Rebasing
Applicant	MYCONE DENTAL SUPPLY CO., INC. 616 HOLLYWOOD AVE. CHERRY HILL, NJ 08002 US Other 510(k) Applications for this Company
Contact	LARRY STEFFIER Other 510(k) Applications for this Contact
Regulation Number	872.3760   More FDA Info for this Regulation Number
Classification Product Code	EBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/08/2003
Decision Date	09/23/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review