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FDA 510(k)

Sysmex Automated Blood Coagulation Analyzer CS-2100i

K-Number: K151259 · 2016-01-26

Decision Date2016-01-26
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Sysmex Automated Blood Coagulation Analyzer CS-2100i is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. It received FDA 510(k) clearance on 2016-01-26 under approval number K151259. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sysmex Automated Blood Coagulation Analyzer CS-2100i?

Sysmex Automated Blood Coagulation Analyzer CS-2100i is a medical device that received FDA 510(k) clearance on 2016-01-26. It is manufactured by Siemens Healthcare Diagnostics Products GmbH. The 510(k) number is K151259.

When was Sysmex Automated Blood Coagulation Analyzer CS-2100i approved by the FDA?

Sysmex Automated Blood Coagulation Analyzer CS-2100i received FDA 510(k) clearance on 2016-01-26, under approval number K151259.

What company makes Sysmex Automated Blood Coagulation Analyzer CS-2100i?

Sysmex Automated Blood Coagulation Analyzer CS-2100i is manufactured by Siemens Healthcare Diagnostics Products GmbH.

What is the FDA product code for Sysmex Automated Blood Coagulation Analyzer CS-2100i?

The FDA product code for Sysmex Automated Blood Coagulation Analyzer CS-2100i is JPA.

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Official Source

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