510(k) K012879

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

K012879 is an FDA 510(k) premarket notification submitted by Exelint Intl. Co. for the device "EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE". The FDA issued a decision of Substantially Equivalent on January 17, 2002. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Exelint Intl. Co. has at least 10 other 510(k) clearances on record.

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