Baxter Healthcare Corp
INTERLINK(TM) BLUNT CANNULA, MODIFICATION
SKU K911868UPC FPA
In Stock
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IIFDA 510(k) Cleared (K911868)
1
Free shipping on orders over $99 · 30-day returns
Baxter Healthcare Corp
Free shipping on orders over $99 · 30-day returns
INTERLINK(TM) BLUNT CANNULA, MODIFICATION is an FDA 510(k)-cleared medical device (K911868) manufactured by Baxter Healthcare Corp. 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 23, 1991. Regulation: 8.
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