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Determining Substantial Equivalence in Premarket Notifications [510(k)] with Different Technological Characteristics; Draft Guidance for Industry and Food and Drug Administration Staff; Availability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Determining Substantial Equivalence in Premarket Notifications [510(k)] with Different Technological Characteristics; Draft Guidance for Industry and Food and Drug Administration Staff; Availability, at the Food and Drug Administration.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.

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1
Comments
1
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closed 4305d ago

Commenters (1)

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