Data Medical Associates, Inc.
CREATININE PROCEDURE
SKU K861655UPC CGX
In Stock
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IIFDA 510(k) Cleared (K861655)
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Free shipping on orders over $99 · 30-day returns
Data Medical Associates, Inc.
Free shipping on orders over $99 · 30-day returns
CREATININE PROCEDURE is an FDA 510(k)-cleared medical device (K861655) manufactured by Data Medical Associates, 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 June 30, 1986. Regulation: 8.
