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

92. 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

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

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

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

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

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

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

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