Dates by Range: 2000 and later - Digital Collections - National Library of Medicine Search Results

Start Over Dates by Range 2000 and later ✖

6131. Peripheral percutaneous transluminal angioplasty (PTA) and specialty catheters: premarket notification (510(k)) submissions : guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, April 14, 2023
Subject(s):: Angioplasty, Balloon, Coronary
Cardiac Catheters
Device Approval
Government Regulation
United States

6132. Medicaid waivers

Author(s):: Mortenson, Logan C., author
Publication:: [Toronto, Ontario] : Thomson Reuters, 19-December-2022
Subject(s):: Medicaid -- legislation & jurisprudence
State Government
Community Health Services -- legislation & jurisprudence
Health Care Reform -- legislation & jurisprudence
Mental Health Services -- legislation & jurisprudence
United States

6133. A risk-based approach to monitoring of clinical investigations questions and answers: guidance for industry

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, April 2023
Subject(s):: Clinical Trials Data Monitoring Committees
Clinical Trials as Topic
Government Regulation
Research Design
Research Personnel
United States

6134. Cybersecurity in medical devices: refuse to accept policy for cyber devices and related systems under section 524B of the FD&C Act : guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, March 30, 2023
Subject(s):: Computer Security -- legislation & jurisprudence
Device Approval
Equipment Safety
Government Regulation
United States
United States.

6135. Soft (hydrophilic) daily wear contact lenses: performance criteria for safety and performance based pathway : guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, March 28, 2023
Subject(s):: Contact Lenses, Hydrophilic -- standards
Device Approval
Equipment Safety
Government Regulation
United States

6136. General considerations for animal studies intended to evaluate medical devices: guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, March 28, 2023
Subject(s):: Animal Experimentation
Animal Welfare
Animals, Laboratory
Device Approval
Equipment Safety
Equipment and Supplies
Government Regulation
United States

6137. Medicaid restructuring

Author(s):: Raduege, Tammy J., author
Publication:: [Toronto, Ontario] : Thomson Reuters, 19-December-2022
Subject(s):: Federal Government
Medicaid -- organization & administration
State Government
United States
United States.

6138. Medicaid reimbursement

Author(s):: Berry, Melissa D., author
Publication:: [Toronto, Ontario] : Thomson Reuters, 19-December-2022
Subject(s):: Federal Government
Insurance, Health, Reimbursement -- legislation & jurisprudence
Medicaid -- legislation & jurisprudence
State Government
United States

6139. Transition plan for medical devices that fall within enforcement policies issued during the coronavirus disease 2019 (COVID-19) public health emergency: guidance for industry, other stakeholders, and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, March 27, 2023
Subject(s):: Equipment and Supplies
Government Regulation
Medical Device Legislation
COVID-19
United States
United States. Food and Drug Administration

6140. Medicaid provider tax

Author(s):: Fleming, Julie A., (Compliance attorney and member of the Minnesota bar), author
Publication:: [Toronto, Ontario] : Thomson Reuters, 19-December-2022
Subject(s):: Federal Government
Medicaid -- legislation & jurisprudence
State Government
Taxes -- legislation & jurisprudence
United States

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