Sequal Technologies, Inc.
OMNI OXYGEN SYSTEM, MODEL 1000
SKU K013931UPC CAW
In Stock
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IIFDA 510(k) Cleared (K013931)
1
Free shipping on orders over $99 · 30-day returns
Sequal Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
OMNI OXYGEN SYSTEM, MODEL 1000 is an FDA 510(k)-cleared medical device (K013931) manufactured by Sequal Technologies, 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 26, 2002. Regulation: 8.
