GE Healthcare said that the U.S. Food and Drug Administration has provided 510(k) clearance for its Innova 3131(IQ) and 2121(IQ) digital flat-panel biplane imaging systems.
The systems cover a patient's lateral and frontal anatomy simultaneously for use in cardiovascular and neurovascular image-guided interventional procedures, according to the Chalfont St. Giles, U.K.-based firm.
The Innova 3131(IQ) and 2121(IQ) products are indicated for use in cardiovascular imaging, diagnostic and interventional procedures, and 3D imaging of vessels and soft tissue, GE said.
By AuntMinnie.com staff writers
March 14, 2006
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