
E.I. Dupont DE Nemours & Co., Inc.
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SR 301 MEDICAL X-RAY FILM is an FDA 510(k)-cleared medical device (K792317) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 8, 1980. Regulation: 8.

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