Acmi Corporation
BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910
SKU K012018UPC GEI
In Stock
—
IIFDA 510(k) Cleared (K012018)
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
Acmi Corporation
Free shipping on orders over $99 · 30-day returns
BICAP COAG BIPOLAR LAPAROSCOPY PROBE, MODEL 006908-910 is an FDA 510(k)-cleared medical device (K012018) manufactured by Acmi Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 2002. Regulation: 8.
