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3. Retained bioburden on surgical instruments after reprocessing: are we just scraping the surface?


4. Emergency use authorization of medical products and related authorities: guidance for industry and other stakeholders


5. Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff


6. Establishing the performance characteristics of in vitro diagnostic devices for the detection or detection and differentiation of human papillomaviruses: guidance for Industry and Food and Drug Administration staff


7. Venous air emboli and automatic contrast media injectors