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Federal Register|December 18, 2018
Medical Device Classification Procedures: Incorporating Food and Drug Administration Safety and Innovation Act Procedures. Final ruleFederal Register|May 16, 2006
Blood vessels recovered with organs and intended for use in organ transplantation. Direct final ruleFederal Register|February 28, 2004
Pediculicide drug products for over-the-counter human use; amendment of final monograph. Final ruleFederal Register|February 28, 2004
Bar code label requirement for human drug products and biological products. Final ruleFederal Register|March 31, 2004
Grants to states for operation of qualified high risk pools. Final ruleFederal Register|March 26, 2004
Drug labeling; orally ingested over-the-counter drug products containing calcium, magnesium, and potassium. Final ruleFederal Register|September 16, 2004
Exemption from import/export requirements for personal medical use. Final ruleFederal Register|July 7, 2005
Revised medical criteria for evaluating genitourinary impairments. Final rulesFederal Register|August 28, 2004
Dental devices; dental noble metal alloys and dental base metal alloys; designation of special controls. Final rulePageof 431