FDA 510(k) Application Details - K033033

Device Classification Name	Light, Operating, Dental   More FDA Info for this Device
510(K) Number	K033033
Device Name	Light, Operating, Dental
Applicant	TRYLON CORP. 970 WEST 190TH ST., SUITE 850 TORRANCE, CA 90502-1037 US Other 510(k) Applications for this Company
Contact	MARTIN L LONKY Other 510(k) Applications for this Contact
Regulation Number	872.4630   More FDA Info for this Regulation Number
Classification Product Code	EAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/26/2003
Decision Date	11/22/2004
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