Biotech Atlantic, Inc.
UNIMARK HOME PREGNANCY TEST DEVICE
SKU K032992UPC LCX
In Stock
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IIFDA 510(k) Cleared (K032992)
1
Free shipping on orders over $99 · 30-day returns
Biotech Atlantic, Inc.
Free shipping on orders over $99 · 30-day returns
UNIMARK HOME PREGNANCY TEST DEVICE is an FDA 510(k)-cleared medical device (K032992) manufactured by Biotech Atlantic, Inc.. 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 20, 2003. Regulation: 8.
