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Med2000 S.R.L.
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MED2000 SPA NEBULIZER ANDYFLOW, MODEL A1/C WITH ACCESSORIES is an FDA 510(k)-cleared medical device (K041327) manufactured by Med2000 S.R.L.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 2004. Regulation: 8.