FDA 510(k) Application Details - K050019

Device Classification Name	Unit, X-Ray, Extraoral With Timer   More FDA Info for this Device
510(K) Number	K050019
Device Name	Unit, X-Ray, Extraoral With Timer
Applicant	KAVO AMERICA 340 EAST MAIN ST. LAKE ZURICH, IL 60047 US Other 510(k) Applications for this Company
Contact	JOHN R MILLER Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	EHD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/05/2005
Decision Date	01/31/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review