MATRIX ELECDT & VACUPULLS

MATRIX ELECDT & VACUPULLS is an FDA 510(k)-cleared medical device (K930264) manufactured by Matrix Electromedical, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 28, 1993. Regulation: 8.