Vanguard Biomedical Corp.
MODIFIED HOMECLINIC PREGNANCY TEST
SKU K895560UPC LCX
In Stock
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IIFDA 510(k) Cleared (K895560)
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Free shipping on orders over $99 · 30-day returns
Vanguard Biomedical Corp.
Free shipping on orders over $99 · 30-day returns
MODIFIED HOMECLINIC PREGNANCY TEST is an FDA 510(k)-cleared medical device (K895560) manufactured by Vanguard Biomedical Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 1989. Regulation: 8.
