FDA 510(k) Application Details - K022953

Device Classification Name	System,X-Ray,Extraoral Source,Digital   More FDA Info for this Device
510(K) Number	K022953
Device Name	System,X-Ray,Extraoral Source,Digital
Applicant	SCHICK TECHNOLOGIES, INC. 30-00 47TH AVE. LONG ISLAND CITY, NY 11101 US Other 510(k) Applications for this Company
Contact	DANIEL MICHAELI Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	MUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/05/2002
Decision Date	10/02/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review