IN VITRO FERRITIN RIA TEST— 510(k) K770702
Substantially EquivalentClinical Assays, Inc.
FDA 510(k) clearance K770702 for IN VITRO FERRITIN RIA TEST, Substantially Equivalent on 1977-06-17. Applicant: Clinical Assays, Inc.. Device class: 2.
Clearance details
- Applicant
- Clinical Assays, Inc.
- Product code
- Code DBF
- Device class
- Class 2
- Regulation
- 21 CFR 866.5340
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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