
H & M Douglas Enterprises, Inc.
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SUN BED BY VERRE ET QUARTZ UVA-FRANCE is an FDA 510(k)-cleared medical device (K833229) manufactured by H & M Douglas Enterprises, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 26, 1984. Regulation: 8.

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