
Coherent Medical Group
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MODEL 5001 MICROMANIPULATOR FOR USE W/TF-25 CO2 is an FDA 510(k)-cleared medical device (K873246) manufactured by Coherent Medical Group. 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 November 9, 1987. Regulation: 8.