FDA 510(k) Application Details - K961049

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K961049
Device Name	Set, Administration, Intravascular
Applicant	LIGHTHOUSE MEDICAL, INC. 100 BEAVER ST. WALTHAM, MA 02154 US Other 510(k) Applications for this Company
Contact	JENNA ANDELMAN Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/15/1996
Decision Date	09/18/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review