Cortek Endoscopy, Inc.
CORTEK URETHEROSCOPE
SKU K000200UPC FGB
In Stock
—
IIFDA 510(k) Cleared (K000200)
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
Cortek Endoscopy, Inc.
Free shipping on orders over $99 · 30-day returns
CORTEK URETHEROSCOPE is an FDA 510(k)-cleared medical device (K000200) manufactured by Cortek Endoscopy, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 2000. Regulation: 8.
Coloplast
SKU MSC612995
Karl Storz Endoscopy
SKU K942112
Coloplast
SKU MSC750215
Coloplast
SKU MSC891872