
Holter-Hausner Intl.
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VALVE, H-H CRUCIFORM SLIT is an FDA 510(k)-cleared medical device (K790126) manufactured by Holter-Hausner Intl.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1979. Regulation: 8.

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