510(k) K142433

Hospira Extension Set by Hospira, Inc. — Product Code FPA

K142433 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "Hospira Extension Set". The FDA issued a decision of Substantially Equivalent on December 8, 2014. 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 8, 2014
Date Received
August 29, 2014
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