FDA 510(k) Application Details - K020470

Device Classification Name	Clip, Implantable   More FDA Info for this Device
510(K) Number	K020470
Device Name	Clip, Implantable
Applicant	BYPASS LTD. 555 THIRTEENTH ST. NW WASHINGTON, DC 20004-1109 US Other 510(k) Applications for this Company
Contact	JONATHAN S KAHAN Other 510(k) Applications for this Contact
Regulation Number	878.4300   More FDA Info for this Regulation Number
Classification Product Code	FZP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/12/2002
Decision Date	03/08/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review