Last synced on 14 November 2025 at 11:06 pm

gi2000 Electrosurgical Generator

Page Type
Cleared 510(K)
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)
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