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Federal Register|August 5, 1998
Natural rubber-containing medical devices; user labeling; cold seal adhesives partial stay--FDA. Final rule
Federal Register|August 7, 1998
Proposed vaccine information materials for hepatitis B, Haemophilus influenzae type b (Hib), Varicella (chickenpox), and measles, mumps, rubella (MMR) vaccines--CDC. Notice with comment period
Federal Register|August 14, 1998
Obstetric and gynecologic devices; reclassification and classification of medical devices used for in vitro fertilization and related assisted reproduction procedures--FDA. Final rule
Federal Register|June 29, 1998
Medical use of byproduct material; public meetings--NRC. Notice of public meetings
Federal Register|June 29, 1998
Medical devices; preemption of state product liability claims--FDA. Withdrawal of proposed rule
Federal Register|July 4, 1998
Medical devices; reclassification and codification of vitamin D test system--FDA. Final rule
Federal Register|July 4, 1998
Medicare program; peer review organization contracts: solicitation of statements of interest from in-state organizations--Alaska, Delaware, the District of Columbia, Hawaii, Idaho, Illinois, Kentucky, Maine, Nebraska, Nevada, South Carolina, Vermont, and Wyoming--HCFA. Notice
Federal Register|July 6, 1998
Medicare and Medicaid programs; surety bond requirements for home health agencies--HCFA. Final rule
Federal Register|July 10, 1998
Revisions to the general safety test requirements for biological products--FDA. Direct final rule: confirmation in part and withdrawal in part
Federal Register|July 12, 1998
Solicitation of information and recommendations for developing OIG compliance program guidance for the durable medical equipment industry--HHS. Notice
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