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Retinalabs.Com
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TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025 is an FDA 510(k)-cleared medical device (K003036) manufactured by Retinalabs.Com. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 21, 2000. Regulation: 8.