
Coherent Medical Group
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COHERENT MARIE ARGON PHOTOCOAGULATOR is an FDA 510(k)-cleared medical device (K893709) manufactured by Coherent Medical Group. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 14, 1989. Regulation: 8.

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