
Recto Molded Products, Inc.
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QUINEVAC II is an FDA 510(k)-cleared medical device (K920629) manufactured by Recto Molded 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 March 23, 1993. Regulation: 8.