The FDA's Ophthalmic Devices Panel is slated to review the pre-market approval application for the Kamra Inlay presbyopia device made by AcuFocus.
The FDA said it plans to hold an advisory panel hearing to evaluate the Kamra Inlay device made by AcuFocus to treat presbyopia, or near vision loss.
The FDA's Ophthalmic Devices Panel will convene June 6 to consider AcuFocus' bid for pre-market approval for the Kamra device, a ring-shaped inlay that's implanted under the surface of the cornea, the federal watchdog agency said today.
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