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Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter

Page Type
Cleared 510(K)
510(k) Number
K190127
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2019
Days to Decision
207 days
Submission Type
Summary

Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheter

Page Type
Cleared 510(K)
510(k) Number
K190127
510(k) Type
Traditional
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2019
Days to Decision
207 days
Submission Type
Summary