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Jostra AG
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JOSTRA VENT CATHETERS, MODELS LV & HKV is an FDA 510(k)-cleared medical device (K022022) manufactured by Jostra AG. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 10, 2002. Regulation: 8.