Phadia AB
AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES
SKU K121156UPC DHB
In Stock
—
IIFDA 510(k) Cleared (K121156)
1
Free shipping on orders over $99 · 30-day returns
Phadia AB
Free shipping on orders over $99 · 30-day returns
AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES is an FDA 510(k)-cleared medical device (K121156) manufactured by Phadia AB. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 2013. Regulation: 8.
