Ameritek Research, LLC
IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT
SKU K050352UPC JTO
In Stock
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IFDA 510(k) Cleared (K050352)
1
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Ameritek Research, LLC
Free shipping on orders over $99 · 30-day returns
IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT is an FDA 510(k)-cleared medical device (K050352) manufactured by Ameritek Research, LLC. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 31, 2005. Regulation: 8.
