FDA 510(k) Application Details - K062130

Device Classification Name	Forceps, Tooth Extractor, Surgical   More FDA Info for this Device
510(K) Number	K062130
Device Name	Forceps, Tooth Extractor, Surgical
Applicant	HAGER & MEISINGER GMBH 7442 S. TUCSON WAY SUITE 130 CENTENNIAL, CO 80112 US Other 510(k) Applications for this Company
Contact	ALEX MILLER Other 510(k) Applications for this Contact
Regulation Number	872.4565   More FDA Info for this Regulation Number
Classification Product Code	EMG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/26/2006
Decision Date	04/16/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review