Draft Guidance for Industry and Food and Drug Administration Staff; Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile

1 organizations filed 1 public comment on Draft Guidance for Industry and Food and Drug Administration Staff; Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile, at the Food and Drug Administration. The comment window closed 3781d ago.

Commenters (1)

• Advanced Medical Technology Associationtrade assoc.

  1 filing · confidence 97%