Automated Blood Coagulation Analyzer CS-2500— 510(k) K172286

Substantially Equivalent

Siemens 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
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
Download summary PDFView on FDA.gov ↗

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Adverse 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.