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2301. Unique device identification: convenience kits : guidance for industry and Food and Drug Administration staff

2302. Requests for feedback and meetings for medical device submissions: the Q-Submission Program : guidance for industry and Food and Drug Administration staff

2303. Utilizing animal studies to evaluate organ preservation devices: guidance for industry and Food and Drug Administration staff

2304. Medical x-ray imaging devices conformance: guidance for industry and Food and Drug Administration staff

2305. Policy clarification for certain fluoroscopic equipment requirements: guidance for industry and Food and Drug Administration staff

2306. 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

2307. Classification and requirements for laser illuminated projectors (LIPs): (Laser Notice No. 57) : guidance for industry and Food and Drug Administration staff

2308. Preparation of food contact notifications for food contact substances in contact with infant formula and/or human milk

2309. Recommendations for reducing the risk of transfusion-transmitted babesiosis