510(k) K103344

INFUSION SETS by Hospira, Inc. — Product Code FPA

K103344 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "INFUSION SETS". The FDA issued a decision of Substantially Equivalent on December 10, 2010. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Hospira, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 2010
Date Received
November 15, 2010
Clearance Type
Special
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