Automated Blood Coagulation Analyzer CS-2500
K-Number: K172286 · 2017-12-18
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.