510(k) K091213

FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMEN by Footprint Medical — Product Code FOS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 2009
Date Received
April 27, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Umbilical Artery
Device Class
Class II
Regulation Number
880.5200
Review Panel
HO
Submission Type