Diagnostic Hybrids, Inc.
DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000
SKU K070206UPC GQW
In Stock
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IIFDA 510(k) Cleared (K070206)
1
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Diagnostic Hybrids, Inc.
Free shipping on orders over $99 · 30-day returns
DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000 is an FDA 510(k)-cleared medical device (K070206) manufactured by Diagnostic Hybrids, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 29, 2007. Regulation: 8.
