Ambu, Inc.
AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR
SKU K042682UPC BTM
In Stock
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IIFDA 510(k) Cleared (K042682)
1
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Ambu, Inc.
Free shipping on orders over $99 · 30-day returns
AMBU SPUR II. ADULT SINGLE PATIENT RESUSCITATOR is an FDA 510(k)-cleared medical device (K042682) manufactured by Ambu, 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 November 14, 2004. Regulation: 8.
