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  1. Regulatory Status
    FDA Class I Device. For In Vitro Diagnostic Use.

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Phase
  1. Life Science Research 13 items
  2. Clinical Research 13 items
Platforms
  1. Plate-Based 6 items
  2. ELISA Instrumentation 5 items
Species
  1. Human 11 items
Brands
  1. Stellux 3 items
Kit Type
  1. Immunoassay Kits 10 items
  2. Kit Component 1 item
  3. Accessory 2 items
  4. Chemiluminescent 3 items
Regulatory Status
  1. FDA 510(k) Cleared. For In Vitro Diagnostic Use 2 items
  2. FDA Class I Device. For In Vitro Diagnostic Use. 13 items
  3. FDA Registered. For In Vitro Diagnostic Use. 34 items
  4. Health Canada Licensed. Not for Sale in the USA. 2 items
  5. Health Canada Licensed 8 items
  6. Research Use Only. Not for Use in Diagnostic Procedures. 561 items
  7. Not Applicable 6 items
Sample Types
  1. EDTA Plasma 1 item
  2. Heparin Plasma 3 items
  3. Plasma 7 items
  4. Serum 10 items
  5. Stool 2 items
  6. Tissue Culture 3 items