510(k) K160870

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

K160870 is an FDA 510(k) premarket notification submitted by Hospira, Inc. for the device "Hospira Administration Sets". The FDA issued a decision of Substantially Equivalent on June 1, 2016. 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
June 1, 2016
Date Received
March 30, 2016
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