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GENII GI 4000 ELECTROSUGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113265
510(k) Type
Traditional
Applicant
Genii, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2012
Days to Decision
139 days
Submission Type
Summary

GENII GI 4000 ELECTROSUGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113265
510(k) Type
Traditional
Applicant
Genii, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2012
Days to Decision
139 days
Submission Type
Summary