FDA 510(k) Application Details - K960843

Device Classification Name	Prosthesis, Nail   More FDA Info for this Device
510(K) Number	K960843
Device Name	Prosthesis, Nail
Applicant	EUROPEAN TOUCH CO., INC. 5203 NORTH 125TH ST. BUTLER, WI 53007 US Other 510(k) Applications for this Company
Contact	MATT WALKER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MQZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/29/1996
Decision Date	08/12/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review