FDA 510(k) Application Details - K131799

Device Classification Name	Cord, Retraction   More FDA Info for this Device
510(K) Number	K131799
Device Name	Cord, Retraction
Applicant	MICROCOPY, DIV. OF NEO-FLO INC. 3120 MOON STATION RD. NW KENNESAW, GA 30144-9017 US Other 510(k) Applications for this Company
Contact	PEGGY GOBER 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	06/19/2013
Decision Date	01/16/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review