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Agilis HisPro Steerable Catheter With Electrodes

Page Type
Cleared 510(K)
510(k) Number
K200721
510(k) Type
Traditional
Applicant
Abbott (St. Jude Medical)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2020
Days to Decision
76 days
Submission Type
Summary

Agilis HisPro Steerable Catheter With Electrodes

Page Type
Cleared 510(K)
510(k) Number
K200721
510(k) Type
Traditional
Applicant
Abbott (St. Jude Medical)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2020
Days to Decision
76 days
Submission Type
Summary