510(k) K905080

MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER by Kendall Healthcare Products Co. Div.Of Tyco Health — Product Code LFJ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 31, 1991
Date Received
November 13, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Subclavian
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type