510(k) K951738

ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER by Sherwood Medical Co. — Product Code FOS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 29, 1995
Date Received
April 14, 1995
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