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FDA 510(k)

BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000

K-Number: K030099 · 2003-06-17

ApplicantBaxter Healthcare Corp
Decision Date2003-06-17
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 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 2003-06-17 under 510(k) number K030099. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000?

BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 is a medical device that received FDA 510(k) clearance on 2003-06-17. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K030099.

When did BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 receive FDA 510(k) clearance?

BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 received FDA 510(k) clearance on 2003-06-17, under 510(k) number K030099.

Who is the listed applicant for BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000?

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 BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000?

The FDA product code for BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 is KDI.

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Related Devices (Code: KDI)

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.

K261267Careflux H60;Careflux H70;Careflux V500Fresenius Medical Care Renal Therapies Group, LLCK252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCK260533ELISIO™-HNipro Medical CorporationK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCK253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLC

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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