
Martin Uram, MD
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E3 MICROPROB SERIES OF LASERS AND ACCESSORIES is an FDA 510(k)-cleared medical device (K000192) manufactured by Martin Uram, MD. 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 April 9, 2000. Regulation: 8.