Datex-Ohmeda Inc., A Division of Instrumentarium C
AESPIRE 7900, AESPIRE VIEW
SKU K092864UPC BSZ
In Stock
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IIFDA 510(k) Cleared (K092864)
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Free shipping on orders over $99 · 30-day returns
Datex-Ohmeda Inc., A Division of Instrumentarium C
Free shipping on orders over $99 · 30-day returns
AESPIRE 7900, AESPIRE VIEW is an FDA 510(k)-cleared medical device (K092864) manufactured by Datex-Ohmeda Inc., A Division of Instrumentarium C. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2010. Regulation: 8.
