This is a legal form that was released by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration on October 1, 2020 and used country-wide. As of today, no separate filing guidelines for the form are provided by the issuing department.
Q: What is FDA3759?
A: FDA3759 refers to Abbreviated Reports on Radiation Safety of Non-medical Ultrasonic Products.
Q: What is the purpose of FDA3759?
A: The purpose of FDA3759 is to provide reports on the radiation safety of non-medical ultrasonic products.
Q: What does FDA3759 cover?
A: FDA3759 covers the radiation safety of non-medical ultrasonic products.
Q: Who issues FDA3759?
A: FDA3759 is issued by the U.S. Food and Drug Administration (FDA).
Q: What is the importance of FDA3759?
A: FDA3759 is important as it ensures the radiation safety of non-medical ultrasonic products.
Q: Who can use FDA3759?
A: FDA3759 can be used by manufacturers, distributors, and users of non-medical ultrasonic products.
Q: Is FDA3759 mandatory?
A: FDA3759 is not mandatory, but it is recommended for non-medical ultrasonic products.
Form Details:
Download a fillable version of Form FDA3759 by clicking the link below or browse more documents and templates provided by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration.