
Dlp, Inc.
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INFANT VENT CATHETER 12001 W/SIDE VENT is an FDA 510(k)-cleared medical device (K834039) manufactured by Dlp, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 2, 1984. Regulation: 8.

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