
Andersen Sterilizers, Inc.
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EOGas 4 Endo-SteriTest RRBI is an FDA 510(k)-cleared medical device (K202879) manufactured by Andersen Sterilizers, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 2021. Regulation: 8.

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