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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2016-06-01 under 510(k) 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. The listed applicant is Hospira, Inc.. The 510(k) number is K160870.

When did Hospira Administration Sets receive FDA 510(k) clearance?

Hospira Administration Sets received FDA 510(k) clearance on 2016-06-01, under 510(k) number K160870.

Who is the listed applicant for Hospira Administration Sets?

The FDA 510(k) record lists Hospira, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hospira Administration Sets?

The FDA product code for Hospira Administration Sets is FPA.

Other records listing Hospira, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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