Kinamed, Inc.
NAVIPRO
SKU K020764UPC HAW
In Stock
—
IIFDA 510(k) Cleared (K020764)
1
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Kinamed, Inc.
Free shipping on orders over $99 · 30-day returns
NAVIPRO is an FDA 510(k)-cleared medical device (K020764) manufactured by Kinamed, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 2, 2002. Regulation: 8.
