PY30, PY60, PY80

PY30, PY60, PY80 is an FDA 510(k)-cleared medical device (K944928) manufactured by Huttinger Medizintechnik GmbH & CO KG. 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 January 26, 1995. Regulation: 8.