
J.J. Consulting Services, Inc.
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UM-D3000/UM-D4000 is an FDA 510(k)-cleared medical device (K963985) manufactured by J.J. Consulting Services, 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 December 26, 1996. Regulation: 8.