
Insight Optical Mfg. Co. of Florida, Inc.
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SPECTACLE FRAME is an FDA 510(k)-cleared medical device (K932802) manufactured by Insight Optical Mfg. Co. of Florida, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 8, 1993. Regulation: 8.

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