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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 the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2022-11-17 under 510(k) 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. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K220558.

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

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

Who is the listed applicant for Blood Administration Sets?

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 Sets?

The FDA product code for Blood Administration Sets 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.

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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