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Fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also please note the regulation entitled Misbranding by reference to premarket notification 21 CFR Part 807. Type of Use Select one or both as applicable Prescription Use Part 21 CFR 801 Subpart D Over-The-Counter Use 21 CFR 801 Subpart C CONTINUE ON A SEPARATE PAGE IF NEEDED. DEPARTMENT OF HEALTH HUMAN SERVICES May 17 2017 Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center -...
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