Draft Guidance for Industry and Food and Drug Administration Staff: The Content of Investigational Device Exemption (IDE) and Premarket Approval (PMA) Applications for Low Glucose Suspend Device Systems

1 organizations filed 2 public comments on Draft Guidance for Industry and Food and Drug Administration Staff: The Content of Investigational Device Exemption (IDE) and Premarket Approval (PMA) Applications for Low Glucose Suspend Device Systems, at the Food and Drug Administration. The comment window closed 5425d ago.

Commenters (1)

• Advanced Medical Technology Associationtrade assoc.

  2 filings · confidence 97%