Automated Blood Coagulation Analyzer CS-2500— 510(k) K172286
Substantially EquivalentSiemens Healthcare Diagnostic Products GmbH
FDA 510(k) clearance K172286 for Automated Blood Coagulation Analyzer CS-2500, Substantially Equivalent on 2017-12-18. Applicant: Siemens Healthcare Diagnostic Products GmbH. Device class: 2.
Clearance details
- Applicant
- Siemens Healthcare Diagnostic Products GmbH
- Product code
- Product code JPA
- Device class
- Class 2
- Regulation
- 21 CFR 864.5425
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Marburg, DE
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More clearances from Siemens Healthcare Diagnostic Products GmbH
view allAdverse events under product code JPA
product code JPA- Death
- 6
- Total
- 6
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.