Sysmex Automated Blood Coagulation Analyzer CS-2100i
K-Number: K151259 · 2016-01-26
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
Other Devices by Siemens Healthcare Diagnostics Products GmbH
Related Devices (Code: JPA)
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.