Clinical Data, Inc.
IN-VITRO TEST FOR THE DETERMINATION OF CREATININE
SKU K854178UPC CGX
In Stock
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IIFDA 510(k) Cleared (K854178)
1
Free shipping on orders over $99 · 30-day returns
Clinical Data, Inc.
Free shipping on orders over $99 · 30-day returns
IN-VITRO TEST FOR THE DETERMINATION OF CREATININE is an FDA 510(k)-cleared medical device (K854178) manufactured by Clinical Data, 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 November 24, 1985. Regulation: 8.
