510(k) K770702— IN VITRO FERRITIN RIA TEST
Substantially EquivalentClinical Assays, Inc.
Clearance details
- Applicant
- Clinical Assays, Inc.
- Product code
- Code DBF
- 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.