
C.D. & F. Corp.
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CORRUGATED TUBING, 770 & 771 is an FDA 510(k)-cleared medical device (K770581) manufactured by C.D. & F. Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 18, 1977. Regulation: 8.

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