FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
Automated Blood Coagulation Analyzer CS-2500
K Number: K172286
·
Decision Dec 18, 2017
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
4
Review Days
143
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Basic Information
- Device Name
- Automated Blood Coagulation Analyzer CS-2500
- K Number
- K172286
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5425
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Siemens Healthcare Diagnostic Products GmbH
- Date Received
- July 28, 2017
- Decision Date
- December 18, 2017
- Product Code
- JPA
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JPA | System, Multipurpose For In Vitro Coagulation Studies | FDA class 2 | Hematology |
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