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Advisor HD Grid Mapping Catheter, Sensor Enabled

Page Type
Cleared 510(K)
510(k) Number
K172393
510(k) Type
Traditional
Applicant
St. Jude Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2018
Days to Decision
258 days
Submission Type
Summary

Advisor HD Grid Mapping Catheter, Sensor Enabled

Page Type
Cleared 510(K)
510(k) Number
K172393
510(k) Type
Traditional
Applicant
St. Jude Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2018
Days to Decision
258 days
Submission Type
Summary