Last synced on 30 September 2022 at 11:05 pm

Cool-tip RF Ablation System E Series

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203150
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2022
Days to Decision
491 days
Submission Type
Summary

Cool-tip RF Ablation System E Series

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203150
510(k) Type
Traditional
Applicant
Covidien LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2022
Days to Decision
491 days
Submission Type
Summary