Biovision AG
MODIFICATION TO VISITOME 20-10 MICROKERATOME
SKU K042083UPC HNO
In Stock
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IFDA 510(k) Cleared (K042083)
1
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Biovision AG
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO VISITOME 20-10 MICROKERATOME is an FDA 510(k)-cleared medical device (K042083) manufactured by Biovision AG. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 15, 2004. Regulation: 8.
