Vortran Medical Technology 1, Inc.
RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000
SKU K001430UPC BTL
In Stock
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IIFDA 510(k) Cleared (K001430)
1
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Vortran Medical Technology 1, Inc.
Free shipping on orders over $99 · 30-day returns
RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000 is an FDA 510(k)-cleared medical device (K001430) manufactured by Vortran Medical Technology 1, 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 July 4, 2000. Regulation: 8.
