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2901. Developing and responding to deficiencies in accordance with the least burdensome provisions: guidance for industry and Food and Drug Administration staff

2902. Requests for feedback on medical device submissions: the pre-submission program and meetings with Food and Drug Administration staff : guidance for industry and Food and Drug Administration staff

2903. Administrative procedures for CLIA categorization: guidance for industry and Food and Drug Administration staff

2904. Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff

2905. M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use

2907. Deciding when to submit a 510(k) for a change to an existing device: guidance for Industry and Food and Drug Administration staff

2908. Deciding when to submit a 510(k) for a software change to an existing device: guidance for industry and Food and Drug Administration staff

2909. De novo classification process (evaluation of automatic class III designation): guidance for industry and Food and Drug Administration staff

2910. Product labeling for certain ultrasonic surgical aspirator devices: guidance for Industry and Food and Drug Administration staff