Last synced on 10 January 2025 at 11:05 pm

FORCETRIAD ELECTROSURGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110268
510(k) Type
Traditional
Applicant
COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2011
Days to Decision
123 days
Submission Type
Summary

FORCETRIAD ELECTROSURGICAL GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110268
510(k) Type
Traditional
Applicant
COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2011
Days to Decision
123 days
Submission Type
Summary