MR Instruments gets clearance for coil suite

MRI coil developer MR Instruments has received U.S. Food and Drug Administration (FDA) 510(k) clearance, the European CE Mark, and Health Canada approval for its 1.5-tesla DuoFlex coil suite.

DuoFlex, which operates on 1.5-tesla MR scanners from GE Healthcare, consists of two 10-cm square paddles, two 24-cm square paddles, and an eight-channel system interface unit, according to the vendor. The flexible paddles can conform to the areas of interest, MR Instruments said.

An optional single-loop array for the coil suite provides access during MRI interventional procedures and would also be of interest to any facility performing pediatric MRI studies, according to the company.

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