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FDA 510(k)

SYSMEX MODEL XT-4000I

K-Number: K091313 · 2010-03-30

Decision Date2010-03-30
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SYSMEX MODEL XT-4000I is the device name listed in this FDA 510(k) record. The listed applicant is Sysmex America, Inc.. It received FDA 510(k) clearance on 2010-03-30 under 510(k) number K091313. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSMEX MODEL XT-4000I?

SYSMEX MODEL XT-4000I is a medical device that received FDA 510(k) clearance on 2010-03-30. The listed applicant is Sysmex America, Inc.. The 510(k) number is K091313.

When did SYSMEX MODEL XT-4000I receive FDA 510(k) clearance?

SYSMEX MODEL XT-4000I received FDA 510(k) clearance on 2010-03-30, under 510(k) number K091313.

Who is the listed applicant for SYSMEX MODEL XT-4000I?

The FDA 510(k) record lists Sysmex America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYSMEX MODEL XT-4000I?

The FDA product code for SYSMEX MODEL XT-4000I is GKZ.

Related Clinical Trials

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.

Other records listing Sysmex America, Inc. as applicant

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.

View all 29 devices →

Related Devices (Code: GKZ)

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.

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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