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FDA Device Info: Guidance for Industry and FDA Staff Intravascular Administration Sets
FDA Device Info: Guidance for Industry and FDA Staff Intravascular Administration Sets
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Request: Guidance for Industry and FDA Staff Intravascular Administration Sets Premarket Notification Submissions 510(k)
Request Year: 2018
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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