510(k) K012879

EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE by Exelint Intl. Co. — Product Code FPA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 17, 2002
Date Received
August 28, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type