TESTOSTERONE RADIOIMMUNOASSY KIT— 510(k) K802135
Substantially EquivalentRadioimmunoassay, Inc.
FDA 510(k) clearance K802135 for TESTOSTERONE RADIOIMMUNOASSY KIT, Substantially Equivalent on 1980-10-10. Applicant: Radioimmunoassay, Inc.. Device class: 1.
Clearance details
- Applicant
- Radioimmunoassay, Inc.
- Product code
- Code CDZ
- Device class
- Class 1
- Regulation
- 21 CFR 862.1680
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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