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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 the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2021-06-10 under 510(k) 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. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K210335.

When did Blood Administration Set receive FDA 510(k) clearance?

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

Who is the listed applicant for Blood Administration Set?

The FDA 510(k) record lists Baxter Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

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 Devices (Code: BRZ)

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.

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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