PERRY SPECIALTIES DESIGNS NEEDLE GUARD

PERRY SPECIALTIES DESIGNS NEEDLE GUARD is an FDA 510(k)-cleared medical device (K932889) manufactured by Perry Specialties Design, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 27, 1996. Regulation: 8.