FDA 510(k) Application Details - K042872

Device Classification Name	Airbrush   More FDA Info for this Device
510(K) Number	K042872
Device Name	Airbrush
Applicant	KAVO AMERICA CORPORATION PO BOX 7007 DEERFIELD, IL 60015 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	872.6080   More FDA Info for this Regulation Number
Classification Product Code	KOJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/18/2004
Decision Date	11/23/2004
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