FDA 510(k) Application Details - K032081

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K032081
Device Name	Powder, Porcelain
Applicant	KAVO AMERICA PO BOX 7007 DEER FIELD, IL 60015 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	872.6660   More FDA Info for this Regulation Number
Classification Product Code	EIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/2003
Decision Date	07/24/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review