Hospira Administration Sets
K-Number: K160870 · 2016-06-01
ApplicantHospira, Inc.
Decision Date2016-06-01
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Hospira Administration Sets is a medical device manufactured by Hospira, Inc.. It received FDA 510(k) clearance on 2016-06-01 under approval number K160870. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Hospira Administration Sets?
Hospira Administration Sets is a medical device that received FDA 510(k) clearance on 2016-06-01. It is manufactured by Hospira, Inc.. The 510(k) number is K160870.
When was Hospira Administration Sets approved by the FDA?
Hospira Administration Sets received FDA 510(k) clearance on 2016-06-01, under approval number K160870.
What company makes Hospira Administration Sets?
Hospira Administration Sets is manufactured by Hospira, Inc..
What is the FDA product code for Hospira Administration Sets?
The FDA product code for Hospira Administration Sets is FPA.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.