FIAX TEST FOR ANTI-RUBELLA ANTIBODY— 510(k) K772219
Substantially EquivalentIdt, A Division of Whittaker M.A. Bioproducts
FDA 510(k) clearance K772219 for FIAX TEST FOR ANTI-RUBELLA ANTIBODY, Substantially Equivalent on 1978-01-20. Applicant: Idt, A Division of Whittaker M.A. Bioproducts.
Clearance details
- Applicant
- Idt, A Division of Whittaker M.A. Bioproducts
- Product code
- Code DHN
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.