Digene Corp.
MODIFICATION TO HYBRID CAPTURE II CT/GC TEST, MODEL 03M90-01
SKU K010891UPC LSK
In Stock
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IFDA 510(k) Cleared (K010891)
1
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Digene Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO HYBRID CAPTURE II CT/GC TEST, MODEL 03M90-01 is an FDA 510(k)-cleared medical device (K010891) manufactured by Digene Corp.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 24, 2001. Regulation: 8.
