Last synced on 12 October 2025 at 8:21 pm

gi2000 Electrosurgical Generator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250657
510(k) Type
Traditional
Applicant
Cintron Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2025
Days to Decision
90 days
Submission Type
Summary

gi2000 Electrosurgical Generator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250657
510(k) Type
Traditional
Applicant
Cintron Medical Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2025
Days to Decision
90 days
Submission Type
Summary