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FDA 510(k)

Sysmex XN-L Automated Hematology Analyzer

K-Number: K182389 · 2019-01-25

Decision Date2019-01-25
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Sysmex XN-L Automated Hematology Analyzer is a medical device manufactured by Sysmex America, Inc.. It received FDA 510(k) clearance on 2019-01-25 under approval number K182389. 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 XN-L Automated Hematology Analyzer?

Sysmex XN-L Automated Hematology Analyzer is a medical device that received FDA 510(k) clearance on 2019-01-25. It is manufactured by Sysmex America, Inc.. The 510(k) number is K182389.

When was Sysmex XN-L Automated Hematology Analyzer approved by the FDA?

Sysmex XN-L Automated Hematology Analyzer received FDA 510(k) clearance on 2019-01-25, under approval number K182389.

What company makes Sysmex XN-L Automated Hematology Analyzer?

Sysmex XN-L Automated Hematology Analyzer is manufactured by Sysmex America, Inc..

What is the FDA product code for Sysmex XN-L Automated Hematology Analyzer?

The FDA product code for Sysmex XN-L Automated Hematology Analyzer is GKZ.

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Official Source

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