Penumbra, Inc.
PENUMBRA EMBOLECTOMY ASPIRATION SYSTEM
SKU K121917UPC QEW
In Stock
—
IIFDA 510(k) Cleared (K121917)
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
Penumbra, Inc.
Free shipping on orders over $99 · 30-day returns
PENUMBRA EMBOLECTOMY ASPIRATION SYSTEM is an FDA 510(k)-cleared medical device (K121917) manufactured by Penumbra, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2012. Regulation: 8.
