FDA 510(k) Applications Submitted by GENII, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K113265 11/04/2011 GENII GI 4000 ELECTROSUGICAL GENERATOR GENII, INC.
K130983 04/09/2013 GENII ARC SMART ARGON PROBE GENII, INC.


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