IN-VITRO TEST FOR THE DETERMINATION OF CREATININE— 510(k) K854178
Substantially EquivalentClinical Data, Inc.
FDA 510(k) clearance K854178 for IN-VITRO TEST FOR THE DETERMINATION OF CREATININE, Substantially Equivalent on 1985-11-25. Applicant: Clinical Data, Inc.. Device class: 2.
Clearance details
- Applicant
- Clinical Data, Inc.
- Product code
- Code CGX
- Device class
- Class 2
- Regulation
- 21 CFR 862.1225
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Recent devices under product code CGX
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