Diagnostic Hybrids, Inc.
D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
SKU K061101UPC GNW
In Stock
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IFDA 510(k) Cleared (K061101)
1
Free shipping on orders over $99 · 30-day returns
Diagnostic Hybrids, Inc.
Free shipping on orders over $99 · 30-day returns
D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT is an FDA 510(k)-cleared medical device (K061101) manufactured by Diagnostic Hybrids, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 19, 2006. Regulation: 8.
