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FDA 510(k)

Blood Administration Set

K-Number: K210335 · 2021-06-10

ApplicantBaxter Healthcare Corporation
Decision Date2021-06-10
Product CodeBRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Blood Administration Set is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2021-06-10 under approval number K210335. 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 Set?

Blood Administration Set is a medical device that received FDA 510(k) clearance on 2021-06-10. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K210335.

When was Blood Administration Set approved by the FDA?

Blood Administration Set received FDA 510(k) clearance on 2021-06-10, under approval number K210335.

What company makes Blood Administration Set?

Blood Administration Set is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for Blood Administration Set?

The FDA product code for Blood Administration Set 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)

K220558Blood Administration SetsBaxter 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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