Beckman Instruments, Inc.
PARAGON ELECTRO. CREATINE KINASE TEST KI
SKU K802826UPC JHX
In Stock
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IIFDA 510(k) Cleared (K802826)
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Free shipping on orders over $99 · 30-day returns
Beckman Instruments, Inc.
Free shipping on orders over $99 · 30-day returns
PARAGON ELECTRO. CREATINE KINASE TEST KI is an FDA 510(k)-cleared medical device (K802826) manufactured by Beckman Instruments, 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 8, 1981. Regulation: 8.
