
H.C.H. Products, Inc.
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APPARATUS, SUCTION, WARD USE, PORTAB- is an FDA 510(k)-cleared medical device (K843750) manufactured by H.C.H. Products, 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 October 10, 1984. Regulation: 8.