C-REACTIVE PROTEIN IMMUNOTURBIDIMETRIC KIT & CRP CALIBRATOR— 510(k) K953212
Substantially EquivalentRandox Laboratories, Ltd.
FDA 510(k) clearance K953212 for C-REACTIVE PROTEIN IMMUNOTURBIDIMETRIC KIT & CRP CALIBRATOR, Substantially Equivalent on 1995-07-31. Applicant: Randox Laboratories, Ltd..
Clearance details
- Applicant
- Randox Laboratories, Ltd.
- Product code
- Code DCK
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crumlin, IE
Data sourced from openFDA. This site is unofficial and independent of the FDA.