Digene Corp.
MODIFICATION HYBRID CAPTURE II CT-ID DNA TEST, MODEL 03M91-01
SKU K010892UPC LSK
In Stock
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IFDA 510(k) Cleared (K010892)
1
Free shipping on orders over $99 · 30-day returns
Digene Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION HYBRID CAPTURE II CT-ID DNA TEST, MODEL 03M91-01 is an FDA 510(k)-cleared medical device (K010892) 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 23, 2001. Regulation: 8.
