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Start Over Formats Text ✖Remove constraint Formats: Text Subjects Equipment and Supplies ✖Remove constraint Subjects: Equipment and Supplies Genre Technical Report ✖Remove constraint Genre: Technical Report

1. Fourth partial report on Project no. 37 -- study of errors in field artillery practice: subject: an analysis of the sources of error in the use of the aiming circle and development of an improved instrument

Author(s):
Hatch, Theodore F., author
Brackett, Frederick S. (Frederick Sumner), 1896-1988, author
Horvath, Steven M., author
Publication:
Fort Knox, Kentucky : Armored Medical Research Laboratory, 28 March 1945
Subject(s):
Military Personnel -- education
Weapons
Equipment and Supplies
United States

5. First partial report on Project no. 45 -- physiological and operational characteristics of T26E3 tank

Author(s):
Brackett, Frederick S. (Frederick Sumner), 1896-1988, author
Nelson, Norton A., author
Roberts, Lester B., author
Mann, Wendell E., author
Walpole, Robert H., author
Publication:
Fort Knox, Kentucky : Armored Medical Research Laboratory, 28 February 1945
Subject(s):
Equipment and Supplies
Weapons
Ventilation
United States

6. Final report on Project no. 45 -- operational and physiological characteristics of the tank T26E3, (M26): subject: the study of the proposed relocation of the 1000 CFM tank ventilating blower to the turret bulge

Author(s):
Walpole, Robert H., author
Nelson, Norton A., author
Palmes, Edward D., author
Publication:
Fort Knox, Kentucky : Armored Medical Research Laboratory, 31 July 1945
Subject(s):
Equipment and Supplies
Weapons
Ventilation
United States

7. Use of real-world evidence to support regulatory decision-making for medical devices: guidance for industry and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, August 31, 2017
Subject(s):
Equipment and Supplies
Equipment Safety
Evidence-Based Medicine
Product Surveillance, Postmarketing
Data Collection
Data Interpretation, Statistical
Decision Making
Device Approval
Quality Control
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

8. FDA categorization of investigational device exemption (IDE) devices to assist the Centers for Medicare and Medicaid Services (CMS) with coverage decisions: guidance for sponsors, clinical investigators, industry, institutional review boards, and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, December 5, 2017
Subject(s):
Device Approval
Equipment and Supplies
Insurance Coverage
Medicare -- economics
Therapies, Investigational
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
Centers for Medicare & Medicaid Services (U.S.)

10. Unique device identification: Policy regarding compliance dates for class I and unclassified devices, direct marking, and Global Unique Device Identification Database requirements for certain devices : guidance for industry and Food and Drug Administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, July 25, 2022
Subject(s):
Databases as Topic
Equipment and Supplies
Government Regulation
Product Labeling
United States
United States. Food and Drug Administration

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Current results range from 1944 to 2023