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IRIDEX Obtained FDA's 510(K) Approval and CE Mark for Non-Invasive Laser Delivery System
Dec 10, 2012IRIDEX has obtained FDA's 510(k) approval and CE mark for its non-invasive laser delivery system, designed for treating serious retinal diseases. Using MicroPulse technology, the new TxCell Scanning laser delivery system saves time in a ...
Tags: IRIDEX, non-invasive, laser delivery system, CE mark approvals
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