FDANonrulemakingFDA-2014-D-0900
Who commented on this docket
Benefit-Risk Factors to Consider When Determining Substantial Equivalence in Premarket Notifications [510(k)] with Different Technological Characteristics; Draft Guidance for Industry and Food and Drug Administration Staff; Availability
1 organizations filed 1 public comment on Benefit-Risk Factors to Consider When Determining Substantial Equivalence in Premarket Notifications [510(k)] with Different Technological Characteristics; Draft Guidance for Industry and Food and Drug Administration Staff; Availability, at the Food and Drug Administration. The comment window closed 4305d ago.
Organizations
1
Comments
1
RIN
—
Comment window
closed 4305d ago
Commenters (1)
- Advanced Medical Technology Associationtrade assoc.1 filing · confidence 97%
Attribution is name-based and imperfect. regulations.gov data is public record.