American Bio Medica Corp.
RAPIDONE-OXY TEST
SKU K014101UPC DJG
In Stock
—
IIFDA 510(k) Cleared (K014101)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
American Bio Medica Corp.
Free shipping on orders over $99 · 30-day returns
RAPIDONE-OXY TEST is an FDA 510(k)-cleared medical device (K014101) manufactured by American Bio Medica Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 2002. Regulation: 8.
