Cliniqa Corporation
LINICAL RF-CRP CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON CX SYSTEMS
SKU K023661UPC JJY
In Stock
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IFDA 510(k) Cleared (K023661)
1
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Cliniqa Corporation
Free shipping on orders over $99 · 30-day returns
LINICAL RF-CRP CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER SYNCHRON CX SYSTEMS is an FDA 510(k)-cleared medical device (K023661) manufactured by Cliniqa Corporation. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 5, 2002. Regulation: 8.
