FDA clears Medicatech DR system

The U.S. Food and Drug Administration (FDA) has cleared the MasteRad digital radiography (DR) system from Medicatech.

MasteRad is a modular system that is completely manufactured in the U.S., according to the company. This reduces shipping taxes, import taxes, and long shipping lead times.

Customers have the choice of an elevating or nonelevating table, manual or motorized movement, and a wide range of DR flat panels in both regular and high definition. What's more, the length and size of MasteRad components can be customized based on available space and individual needs of clients.

The system also includes Voyance, acquisition software that contains advanced tools, one-page design, and fast database search.

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