SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES
K-Number: K061150 · 2006-07-06
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Device Summary
Frequently Asked Questions
What is the SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES?
SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES is a medical device that received FDA 510(k) clearance on 2006-07-06. The listed applicant is Sysmex America, Inc.. The 510(k) number is K061150.
When did SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES receive FDA 510(k) clearance?
SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES received FDA 510(k) clearance on 2006-07-06, under 510(k) number K061150.
Who is the listed applicant for SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES?
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 AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES?
The FDA product code for SYSMEX AUTOMATED HEMATOLOGY ANALYZER, XT-SERIES 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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