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  1. Category
    Plate-Based
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    Instruments
  3. Regulatory Status
    FDA 510(k) Cleared. For In Vitro Diagnostic Use

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Regulatory Status
  1. FDA 510(k) Cleared. For In Vitro Diagnostic Use 1 item
  2. FDA Class I Device. For In Vitro Diagnostic Use. 6 items
  3. FDA Registered. For In Vitro Diagnostic Use. 22 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. 252 items
  7. Not Applicable 7 items