FDA-USER FEES & REFU › User Fees and Refunds for Premarket Notification Submissions (510(k)s - Guidance for Industry and Food and Drug Administration Staff

FDA-USER FEES & REFU - 2017 EDITION - CURRENT
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User Fees and Refunds for Premarket Notification Submissions (510(k)s - Guidance for Industry and Food and Drug Administration Staff


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Document Number

FDA-USER FEES & REFU

Revision Level

2017 EDITION

Status

Current

Publication Date

Oct. 2, 2017

Page Count

14 pages