Peak Surgical, Inc.
PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES
SKU K082786UPC GEI
In Stock
—
IIFDA 510(k) Cleared (K082786)
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
Peak Surgical, Inc.
Free shipping on orders over $99 · 30-day returns
PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICES is an FDA 510(k)-cleared medical device (K082786) manufactured by Peak Surgical, 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 December 2, 2008. Regulation: 8.
