
Oscor Medical Corp.
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HEMOSTASIS VALVE, WITH OR WITHOUT SIDE PORT is an FDA 510(k)-cleared medical device (K890277) manufactured by Oscor Medical 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 March 9, 1989. Regulation: 8.

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