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Titles
- Interpretation of and compliance policy for certain label requirement: applicability of certain Federal Food, Drug, and Cosmetic Act requirements to vape shops2
- Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion1
- Compliance policy for required warning statements on small-packaged cigars1
- Deciding when to submit a 510(k) for a change to an existing device: guidance for Industry and Food and Drug Administration staff1
- Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff1
- Extension of certain tobacco product compliance deadlines related to the final deeming rule: (revised)1
- Food labeling: serving sizes of foods that can reasonably be consumed at one eating occasion, reference amounts customarily consumed, serving size-related issues, dual-column labeling, and miscellaneous topics1
- Medical product communications that are consistent with the FDA-required labeling: questions and answers1
- Metal expandable biliary stents: premarket notification (510(k)) submissions : guidance for industry and Food and Drug Administration Staff1
- Pediatric information for x-ray imaging device premarket notifications: guidance for industry and Food and Drug Administration staff1
- Pediatric information incorporated into human prescription drug and biological product labeling1
- Product labeling for certain ultrasonic surgical aspirator devices: guidance for Industry and Food and Drug Administration staff1
- Product name placement, size, and prominence in promotional labeling and advertisements1
- Registration and product listing for owners and operators of domestic tobacco product establishments: (revised)1
- Technical considerations for additive manufactured medical devices: guidance for industry and Food and Drug Administration staff1
- Unique device identification: convenience kits : guidance for industry and Food and Drug Administration staff1
- Unique device identification: direct marking of devices : guidance for Industry and Food and Drug administration staff1
- Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff1