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FDA 510(k)

SYNTRA + DIALYZER, MODEL 200

K-Number: K023664 · 2003-02-21

ApplicantBaxter Healthcare Corp
Decision Date2003-02-21
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYNTRA + DIALYZER, MODEL 200 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 2003-02-21 under 510(k) number K023664. 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 SYNTRA + DIALYZER, MODEL 200?

SYNTRA + DIALYZER, MODEL 200 is a medical device that received FDA 510(k) clearance on 2003-02-21. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K023664.

When did SYNTRA + DIALYZER, MODEL 200 receive FDA 510(k) clearance?

SYNTRA + DIALYZER, MODEL 200 received FDA 510(k) clearance on 2003-02-21, under 510(k) number K023664.

Who is the listed applicant for SYNTRA + DIALYZER, MODEL 200?

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 SYNTRA + DIALYZER, MODEL 200?

The FDA product code for SYNTRA + DIALYZER, MODEL 200 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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