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Business · 15/02/2006

FDA Releases Guidance for Implantable Intra-Aneurysm Pressure Measurement Systems

The Food and Drug Administration (FDA) has released a guidance document outlining the requirements for implantable intra-aneurysm pressure measurement systems, which are classified as Class II devices subject to special controls. The document is effective immediately and open to public comment.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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