SYSMEX MODEL XT-4000I
K-Number: K091313 · 2010-03-30
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Device Summary
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.
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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