The US Food and Drug Administration plans to hold an in-person meeting of its Ophthalmic Devices Panel on 9 June in Gaithersburg, MD. While the device center has either canceled, postponed or decided to webcast all other meetings since the COVID-19 crisis began, the meeting announcement seems to be an indication the agency is hoping to make a return to normal operations in two months.
On 1 April the Center for Devices and Radiological Health (CDRH) posted its plans to call on its advisory committee of ophthalmic experts to discuss and consider whether or not to recommend approval of Refocus Group
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