Business · 26/04/2010Updated: 10/17/2026 · 1 min read
FDA Publishes Draft Guidance for Infusion Pump Premarket Notifications
Summary
The Food and Drug Administration has released a draft guidance document to enhance the safety and effectiveness of infusion pumps, which are devices that require a 510(k) premarket notification submission.
Original source language: Federal Register — Health and Human ServicesOpen original release →