FDA 510(k) Application Details - K033660

Device Classification Name	Clip, Scalp   More FDA Info for this Device
510(K) Number	K033660
Device Name	Clip, Scalp
Applicant	RUDOLF STORZ GMBH AMSTEL 320-1 AMSTERDAM 1017AP NL Other 510(k) Applications for this Company
Contact	ANGELIKA SCHERP Other 510(k) Applications for this Contact
Regulation Number	882.4150   More FDA Info for this Regulation Number
Classification Product Code	HBO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/21/2003
Decision Date	01/07/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review