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FDA 510(k)

Blood Administration Sets

K-Number: K220558 · 2022-11-17

ApplicantBaxter Healthcare Corporation
Decision Date2022-11-17
Product CodeBRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Blood Administration Sets is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2022-11-17 under approval number K220558. The device is classified under product code BRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Blood Administration Sets?

Blood Administration Sets is a medical device that received FDA 510(k) clearance on 2022-11-17. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K220558.

When was Blood Administration Sets approved by the FDA?

Blood Administration Sets received FDA 510(k) clearance on 2022-11-17, under approval number K220558.

What company makes Blood Administration Sets?

Blood Administration Sets is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for Blood Administration Sets?

The FDA product code for Blood Administration Sets is BRZ.

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Related PubMed Literature

PMID: 41501972 First Application of an Eddy-Scale Hemolysis Model to the Food and Drug Administration Nozzle Using Computational Fluid Dynamics. ASAIO journal (American Society for Artificial Internal Organs : 1992) (2026)

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Related Devices (Code: BRZ)

K210335Blood Administration SetBaxter Healthcare Corporation

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.

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