READI-STRAND; MODEL PSSTRAND

READI-STRAND; MODEL PSSTRAND is an FDA 510(k)-cleared medical device (K020337) manufactured by Worldwide Medical Technologies, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 28, 2002. Regulation: 8.