Menlo Care, Inc.
LANDMARK(TM) VENOUS ACCESS DEVICE
SKU K882242UPC FOZ
In Stock
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IIFDA 510(k) Cleared (K882242)
1
Free shipping on orders over $99 · 30-day returns
Menlo Care, Inc.
Free shipping on orders over $99 · 30-day returns
LANDMARK(TM) VENOUS ACCESS DEVICE is an FDA 510(k)-cleared medical device (K882242) manufactured by Menlo Care, Inc.. 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 19, 1988. Regulation: 8.
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