
Cordis Corp.
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CORDIS BRITE TIP CATHETER SHEATH INTRODUCER SYSTEM is an FDA 510(k)-cleared medical device (K984500) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 22, 1998. Regulation: 8.

ADC
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