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FDA 510(k)

Automated Blood Coagulation Analyzer CS-2500

K-Number: K172286 · 2017-12-18

Decision Date2017-12-18
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Automated Blood Coagulation Analyzer CS-2500 is a medical device manufactured by Siemens Healthcare Diagnostic Products GmbH. It received FDA 510(k) clearance on 2017-12-18 under approval number K172286. 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 Automated Blood Coagulation Analyzer CS-2500?

Automated Blood Coagulation Analyzer CS-2500 is a medical device that received FDA 510(k) clearance on 2017-12-18. It is manufactured by Siemens Healthcare Diagnostic Products GmbH. The 510(k) number is K172286.

When was Automated Blood Coagulation Analyzer CS-2500 approved by the FDA?

Automated Blood Coagulation Analyzer CS-2500 received FDA 510(k) clearance on 2017-12-18, under approval number K172286.

What company makes Automated Blood Coagulation Analyzer CS-2500?

Automated Blood Coagulation Analyzer CS-2500 is manufactured by Siemens Healthcare Diagnostic Products GmbH.

What is the FDA product code for Automated Blood Coagulation Analyzer CS-2500?

The FDA product code for Automated Blood Coagulation Analyzer CS-2500 is JPA.

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Official Source

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