
Medical Technology Specialists, Inc.
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PRO2 CHECK OXYGEN INDICATOR is an FDA 510(k)-cleared medical device (K983500) manufactured by Medical Technology Specialists, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 16, 1999. Regulation: 8.

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