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

Page Type
Cleared 510(K)
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)
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