For instance, the Safe Medical Devices Act of 1990 included design validation requirements for medical device manufacturers.
What does SMDA stand for?
SMDA stands for Safe Medical Devices Act
This definition appears frequently and is found in the following Acronym Finder categories:
- Science, medicine, engineering, etc.
See other definitions of SMDA
We have 26 other meanings of SMDA in our Acronym Attic
- Syndicat Mixte du Dijonnais (French: Union Meeting of Dijon; France)
- Syndrome Myélodysplasique (French: Myelodysplastic Syndrome)
- System Management Daemon (Unix)
- Système Métrique Décimal (French: Metric Decimal System)
- Systems Management Director/Directorate
- Systems Management Division (Intel)
- Staff Management Division, Office of the Chief of Staff, Army
- Space and Missile Defense - Technical Center (US Army)
- SMD/ADP & Telecommunications Branch
- SMD/Infrastructure Management Branch
- Schenectady Metroplex Development Authority (Schenectady, NY)
- Scrap Metal Dealers Act (UK)
- Second Marine Division Association
- Southern Maine Dressage Association
- Spring Mountain District Association (winemakers; California)
- Sprint Modeling Data Analysis
- Single MAC Dual Attached Concentrator
- School met de Bijbel (Dutch: School with the Bible)
- Servicing Mission Data Base (NASA)
- Short Message Delivery Broadcast
Samples in periodicals archive:
In Congress, he has supported landmark health legislation such as the Ryan White Comprehensive AIDS Resources Emergency Act, the Nutrition Labeling and Education Act, the Breast and Cervical Cancer Mortality Prevention Act, the Safe Medical Devices Act, the Patent Term Restoration and Drug Competition Act and the Orphan Drug Act.
And finally, the Safe Medical Devices Act of 1990 (SMDA) requires healthcare facilities to report deaths, serious illnesses, and injuries associated with the use of medical devices.
He was also key participant in drafting the Safe Medical Devices Act of 1990.
Before Congress passed the Medical Device Amendments of 1976, the device industry hadn't been regulated at all, and until the Safe Medical Devices Act passed in 1990, the FDA's Center for Devices and Radiological Health paid scant attention to low- and medium-risk devices.
] Safe Medical Devices Act of 1990, Public Law 101-629 [HR 3095]; 28 November 1990, Section 519 (21 U.
FDA, through this experience and with the mandate of the Safe Medical Devices Act, very likely will establish more rigorous requirements for the so-called 510K devices.
NCS' new medical device tracking application provides a cost-effective solution to help manufacturers comply with the Safe Medical Devices Act of 1990 as well as the tracking regulations issued by the FDA.