510(k) K853283

VACCESS TM 4006 by Vas-Cath of Canada , Ltd. — Product Code LFJ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 22, 1985
Date Received
August 5, 1985
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