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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 the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostic Products GmbH. It received FDA 510(k) clearance on 2017-12-18 under 510(k) 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. The listed applicant is Siemens Healthcare Diagnostic Products GmbH. The 510(k) number is K172286.

When did Automated Blood Coagulation Analyzer CS-2500 receive FDA 510(k) clearance?

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

Who is the listed applicant for Automated Blood Coagulation Analyzer CS-2500?

The FDA 510(k) record lists Siemens Healthcare Diagnostic Products GmbH as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Siemens Healthcare Diagnostic Products GmbH 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: JPA)

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

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