Critikon Company, LLC
RATEMINDER(TM) V INFUSION PUMP, MODIFICATION
SKU K911769UPC FRN
In Stock
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IIFDA 510(k) Cleared (K911769)
1
Free shipping on orders over $99 · 30-day returns
Critikon Company, LLC
Free shipping on orders over $99 · 30-day returns
RATEMINDER(TM) V INFUSION PUMP, MODIFICATION is an FDA 510(k)-cleared medical device (K911769) manufactured by Critikon Company, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 2, 1991. Regulation: 8.
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