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FDA 510(k)

MODIFIED BLOOD RECIPIENT SET

K-Number: K993120 · 1999-11-17

ApplicantBaxter Healthcare Corp
Decision Date1999-11-17
Product CodeBRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED BLOOD RECIPIENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1999-11-17 under 510(k) number K993120. 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 MODIFIED BLOOD RECIPIENT SET?

MODIFIED BLOOD RECIPIENT SET is a medical device that received FDA 510(k) clearance on 1999-11-17. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K993120.

When did MODIFIED BLOOD RECIPIENT SET receive FDA 510(k) clearance?

MODIFIED BLOOD RECIPIENT SET received FDA 510(k) clearance on 1999-11-17, under 510(k) number K993120.

Who is the listed applicant for MODIFIED BLOOD RECIPIENT SET?

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

What is the FDA product code for MODIFIED BLOOD RECIPIENT SET?

The FDA product code for MODIFIED BLOOD RECIPIENT 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 CorporationK210335Blood Administration SetBaxter Healthcare CorporationK132905200 MICRON BLOOD COMPONENT FILTER AND SYRINGE ADAPTERArteriocyte Medical Systems, Inc.K083349BLOOD TRANSFUSION SETShan Dong Wei Gao Group Medical Polymer ProductsK073339BLOOD COMPONENT RECIPIENT SET WITH STANDARD SIZE FILTER AND INFUSION SET WITH SIDE ARM LUER CONNECTORFenwal, Inc.K041496PENTATRASFU BLOOD TRANSFUSION SETSPentaferte S.P.A

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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