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381. Policy clarification for certain fluoroscopic equipment requirements: guidance for industry and Food and Drug Administration staff

382. Laser products: conformance with IEC 60825-1 Ed. 3 and IEC 60601-2-22 Ed. 3.1 : (Laser Notice No. 56) : guidance for industry and Food and Drug Administration staff

383. Classification and requirements for laser illuminated projectors (LIPs): (Laser Notice No. 57) : guidance for industry and Food and Drug Administration staff

384. Preparation of food contact notifications for food contact substances in contact with infant formula and/or human milk

385. Recommendations for reducing the risk of transfusion-transmitted babesiosis

387. Maximal usage trials for topically applied active ingredients being considered for inclusion in an over-the -counter monograph: study elements and considerations

388. Oncology pharmaceuticals: reproductive toxicity testing and labeling recommendations

389. Considerations in demonstrating interchangeability with a reference product

390. FDA deems certain tobacco products subject to FDA authority, sales and distribution restrictions, and health warning requirements for packages and advertisements: (revised)