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

282. Manufacturers sharing patient-specific information from medical devices with patients upon request: guidance for industry and Food and Drug Administration staff

283. Formal dispute resolution: sponsor appeals above the division level : guidance for industry and review staff : good review practice

285. Chronic hepatitis C virus infection: developing direct-acting antiviral drugs for treatment

286. Recurrent herpes labialis: developing drugs for treatment and prevention

287. Evaluating drug effects on the ability to operate a motor vehicle

288. Regulatory considerations for human cells, tissues, and cellular and tissue-based products: minimal manipulation and homologous use : guidance for industry and Food and Drug Administration staff

289. Same surgical procedure exception under 21 CFR 1271.15(b): questions and answers regarding the scope of the exception

290. Unique device identification: direct marking of devices : guidance for Industry and Food and Drug administration staff