October 14, 2004
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Laser for glaucoma, retinal disorders granted U.S. marketing approval

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MOUNTAIN VIEW, Calif. — An infrared diode laser photocoagulator for use in treating retinal disorders and glaucoma has been granted 501(k) marketing approval by the Food and Drug Administration, the laser’s marketer announced in a press release.

The Iris Medical IQ 810 has been designed to perform traditional and minimum intensity photocoagulation, said marketer Iridex in the press release.

Features of the IQ 810 include interactive software for setup and operation of the machine, customization of laser output and settings, and an integrated systems diagnostic. The software offers ophthalmologists “quick access” to several operating modes and advanced pulse modalities, Iridex noted.

The laser is commercially available now and will be featured at the Iridex booth next week at the American Academy of Ophthalmology meeting.