Stryker Corporation
STYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM
SKU K112593UPC ERL
In Stock
—
IIFDA 510(k) Cleared (K112593)
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
Stryker Corporation
Free shipping on orders over $99 · 30-day returns
STYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM is an FDA 510(k)-cleared medical device (K112593) manufactured by Stryker Corporation. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 30, 2012. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
Ohmeda Medical
SKU K871399
Insulet Corporation
SKU K182630