Biotrack, Inc.
BIOTRACK PROTIME CONTROLS (BIOTRACK PROTIME TEST)
SKU K860719UPC JPA
In Stock
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IIFDA 510(k) Cleared (K860719)
1
Free shipping on orders over $99 · 30-day returns
Biotrack, Inc.
Free shipping on orders over $99 · 30-day returns
BIOTRACK PROTIME CONTROLS (BIOTRACK PROTIME TEST) is an FDA 510(k)-cleared medical device (K860719) manufactured by Biotrack, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 1986. Regulation: 8.
