510(k) K142367

Hospira Primary Sets by Hospira, Inc. — Product Code FPA

K142367 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "Hospira Primary Sets". The FDA issued a decision of Substantially Equivalent on November 25, 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
November 25, 2014
Date Received
August 25, 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