510(k) K142622

IV Administration by Hospira, Inc. — Product Code FPA

K142622 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "IV Administration". The FDA issued a decision of Substantially Equivalent on January 15, 2015. 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
January 15, 2015
Date Received
September 16, 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