Leica Biosystems Imaging, Inc.
Aperio GT 450 DX
SKU K232202UPC PSY
In Stock
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IIFDA 510(k) Cleared (K232202)
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Free shipping on orders over $99 · 30-day returns
Leica Biosystems Imaging, Inc.
Free shipping on orders over $99 · 30-day returns
Aperio GT 450 DX is an FDA 510(k)-cleared medical device (K232202) manufactured by Leica Biosystems Imaging, Inc.. This device is classified under the Pathology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 15, 2024. Regulation: 8.
