Keystone Diagnostics, Inc.
MODIFICATION TO KDI QUIK TEST MARIJUANA SCREEN
SKU K875219UPC LDJ
In Stock
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IIFDA 510(k) Cleared (K875219)
1
Free shipping on orders over $99 · 30-day returns
Keystone Diagnostics, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO KDI QUIK TEST MARIJUANA SCREEN is an FDA 510(k)-cleared medical device (K875219) manufactured by Keystone Diagnostics, Inc.. 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 June 23, 1988. Regulation: 8.
