
Qmed, Inc.
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A.R.M. (ASPEN RETURN MONITOR) is an FDA 510(k)-cleared medical device (K873591) manufactured by Qmed, 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 September 29, 1987. Regulation: 8.