TIA CRP TEST KIT— 510(k) K914155
Substantially EquivalentCrestat Diagnostics, Inc.
FDA 510(k) clearance K914155 for TIA CRP TEST KIT, Substantially Equivalent on 1992-01-15. Applicant: Crestat Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- Crestat Diagnostics, Inc.
- Product code
- Code DCK
- Device class
- Class 2
- Regulation
- 21 CFR 866.5270
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Torrance, CA, US
Recent devices under product code DCK
view allMore clearances from Crestat Diagnostics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.