FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Hospira Sapphire Sets

K Number: K160492 · Decision Dec 6, 2016
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
47
Applicant Total
45
Review Days
288

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Basic Information

Device Name
Hospira Sapphire Sets
K Number
K160492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hospira, Inc.
Date Received
February 22, 2016
Decision Date
December 6, 2016
Product Code
MRZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MRZ Accessories, Pump, Infusion

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MRZ), ordered by most recent decision date.

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Other Clearances by Hospira, Inc.

K Number Device Name
K161469 Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play Module
K161036 Hospira Extension Set, Hospira Primary Set
K160870 Hospira Administration Sets
K143612 LifeCare PCA Infusion System
K143087 Hospira Blood Set
K143015 Hospira Primary Sets
K141789 PLUM 360 INFUSION SYSTEM WITH HOSPIRA MEDNET, SMART CARD PLUG N PLAY CE 3.0 MODULE FOR PLUM A+ INFUSION SYSTEM UPGRADE
K142622 IV Administration
K142974 Extension Sets
K142433 Hospira Extension Set
Search all 45 clearances from Hospira, Inc. →