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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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