
Resect Medical, Inc.
Free shipping on orders over $99 · 30-day returns
RESECT MEDICAL INLINE BI-POLAR RF LINEAR COAGULATION DEVICE is an FDA 510(k)-cleared medical device (K040763) manufactured by Resect Medical, Inc.. 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 April 7, 2004. Regulation: 8.