T3 UPTAKE DIAGNOSTIC KIT— 510(k) K821722
Substantially EquivalentDiagnostic Reagents, Inc.
FDA 510(k) clearance K821722 for T3 UPTAKE DIAGNOSTIC KIT, Substantially Equivalent on 1982-06-24. Applicant: Diagnostic Reagents, Inc..
Clearance details
- Applicant
- Diagnostic Reagents, Inc.
- Product code
- Code KHQ
- Advisory panel
- Clinical Chemistry
- 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.