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Reprocessed Inquiry Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
510(k) Number
K171277
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2017
Days to Decision
175 days
Submission Type
Summary

Reprocessed Inquiry Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
510(k) Number
K171277
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2017
Days to Decision
175 days
Submission Type
Summary