STERIS Corporation
VERIFY STEAM INDICATORS, MODELS 250F 25, 250F 30, 270F 15, 270F 3-10 AND 270F 4
SKU K070461UPC JOJ
In Stock
—
IIFDA 510(k) Cleared (K070461)
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
STERIS Corporation
Free shipping on orders over $99 · 30-day returns
VERIFY STEAM INDICATORS, MODELS 250F 25, 250F 30, 270F 15, 270F 3-10 AND 270F 4 is an FDA 510(k)-cleared medical device (K070461) manufactured by STERIS Corporation. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 2007. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
Ohmeda Medical
SKU K871399
Insulet Corporation
SKU K182630