
Senorx, Inc.
Free shipping on orders over $99 · 30-day returns
GEL MARK BIOPSY SITE MARKER, MODELS MKOOO1, MK0004, MK0007 is an FDA 510(k)-cleared medical device (K000060) manufactured by Senorx, 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 March 26, 2000. Regulation: 8.