510(k) K941814

ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER by Sherwood Medical Co. — Product Code FOS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 30, 1994
Date Received
April 12, 1994
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