Ventlab Corp.
V*CARE MANUAL RESUSCITATOR
SKU K012842UPC BTM
In Stock
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IIFDA 510(k) Cleared (K012842)
1
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Ventlab Corp.
Free shipping on orders over $99 · 30-day returns
V*CARE MANUAL RESUSCITATOR is an FDA 510(k)-cleared medical device (K012842) manufactured by Ventlab Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2001. Regulation: 8.
