FDA 510(k) Application Details - K100653

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K100653
Device Name	Resin, Denture, Relining, Repairing, Rebasing
Applicant	LANG DENTAL MFG. CO., INC. 175 MESSNER DR. WHEELING, IL 60090-0969 US Other 510(k) Applications for this Company
Contact	DAVID LANG 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	03/08/2010
Decision Date	10/08/2010
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