Covidien Lp, Formerly Registered AS United States
SILS STITCH ENDOSCOPIC SUTURING DEVICE
SKU K090419UPC OCW
In Stock
—
IIFDA 510(k) Cleared (K090419)
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
Covidien Lp, Formerly Registered AS United States
Free shipping on orders over $99 · 30-day returns
SILS STITCH ENDOSCOPIC SUTURING DEVICE is an FDA 510(k)-cleared medical device (K090419) manufactured by Covidien Lp, Formerly Registered AS United States. 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 8, 2009. Regulation: 8.
Coloplast
SKU MSC612995
Karl Storz Endoscopy
SKU K942112
Coloplast
SKU MSC750215
Coloplast
SKU MSC891872