Beckman Coulter, Inc.
ACCESS FOLATE ASSAY (MODIFICATION)
SKU K955434UPC CGN
In Stock
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IIFDA 510(k) Cleared (K955434)
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Free shipping on orders over $99 · 30-day returns
Beckman Coulter, Inc.
Free shipping on orders over $99 · 30-day returns
ACCESS FOLATE ASSAY (MODIFICATION) is an FDA 510(k)-cleared medical device (K955434) manufactured by Beckman Coulter, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 28, 1996. Regulation: 8.
