IN-VITRO TEST DETERMINATION OF URIC ACID— 510(k) K854185
Substantially EquivalentClinical Data, Inc.
FDA 510(k) clearance K854185 for IN-VITRO TEST DETERMINATION OF URIC ACID, Substantially Equivalent on 1985-11-25. Applicant: Clinical Data, Inc.. Device class: 1.
Clearance details
- Applicant
- Clinical Data, Inc.
- Product code
- Code KNK
- Device class
- Class 1
- Regulation
- 21 CFR 862.1775
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Recent devices under product code KNK
view allMore clearances from Clinical Data, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.