Bausch & Lomb, Inc.
AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28
SKU K063694UPC KYB
In Stock
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IFDA 510(k) Cleared (K063694)
1
Free shipping on orders over $99 · 30-day returns
Bausch & Lomb, Inc.
Free shipping on orders over $99 · 30-day returns
AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28 is an FDA 510(k)-cleared medical device (K063694) manufactured by Bausch & Lomb, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 6, 2007. Regulation: 8.
