Siemens Elema AB
MODIFICATION TO KION ANESTHESIA SYSTEM
SKU K001315UPC BSZ
In Stock
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IIFDA 510(k) Cleared (K001315)
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Free shipping on orders over $99 · 30-day returns
Siemens Elema AB
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO KION ANESTHESIA SYSTEM is an FDA 510(k)-cleared medical device (K001315) manufactured by Siemens Elema AB. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 25, 2000. Regulation: 8.
