HUMAN GROWTH HORMONE IMMUNORADIOMETRIC ASSAY KIT— 510(k) K851259
Substantially EquivalentNichols Institute Diagnostics
FDA 510(k) clearance K851259 for HUMAN GROWTH HORMONE IMMUNORADIOMETRIC ASSAY KIT, Substantially Equivalent on 1985-05-13. Applicant: Nichols Institute Diagnostics. Device class: 1.
Clearance details
- Applicant
- Nichols Institute Diagnostics
- Product code
- Code CFL
- Device class
- Class 1
- Regulation
- 21 CFR 862.1370
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
Recent devices under product code CFL
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Data sourced from openFDA. This site is unofficial and independent of the FDA.