Quinton, Inc.
PERITONEAL CATHETER-CHANGES-
SKU K833749UPC FKX
In Stock
—
IIFDA 510(k) Cleared (K833749)
1
Free shipping on orders over $99 · 30-day returns
Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
PERITONEAL CATHETER-CHANGES- is an FDA 510(k)-cleared medical device (K833749) manufactured by Quinton, 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 December 26, 1983. Regulation: 8.
