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REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 60CM, REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 100CM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131614
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2013
Days to Decision
87 days
Submission Type
Summary

REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 60CM, REPROCESSED CLOSUREFAST RADIOFREQUENCY CATHETER 100CM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131614
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2013
Days to Decision
87 days
Submission Type
Summary