Device Labs, Inc.
PERCUTANEOUS INTRODUCER KIT
SKU K902135UPC FOZ
In Stock
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IIFDA 510(k) Cleared (K902135)
1
Free shipping on orders over $99 · 30-day returns
Device Labs, Inc.
Free shipping on orders over $99 · 30-day returns
PERCUTANEOUS INTRODUCER KIT is an FDA 510(k)-cleared medical device (K902135) manufactured by Device Labs, 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 July 31, 1990. Regulation: 8.
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