FDA 510(k) Application Details - K101756

Device Classification Name	Cord, Retraction   More FDA Info for this Device
510(K) Number	K101756
Device Name	Cord, Retraction
Applicant	KERR CORPORATION 1717 WEST COLLINS AVENUE ORANGE, CA 92867 US Other 510(k) Applications for this Company
Contact	Wendy Garman Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MVL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/23/2010
Decision Date	10/26/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review