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Tecnimed S.R.L.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO THERMOFOCUS 0800, 0900, 01500 AND 0700 SERIES is an FDA 510(k)-cleared medical device (K072108) manufactured by Tecnimed S.R.L.. 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 August 30, 2007. Regulation: 8.

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