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Zdrowie i gospodarka · 28/06/2013

FDA Releases Draft Guidance on Implanted Blood Access Devices for Hemodialysis

The Food and Drug Administration (FDA) has made available a draft guidance document to aid in the reclassification of implanted blood access devices for hemodialysis, which is currently under consideration for class II (special controls) status.

Source: Federal Register — Food and Drug AdministrationOpen original release →