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Reprocessed Inquiry Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
510(k) Number
K203261
510(k) Type
Special
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2021
Days to Decision
120 days
Submission Type
Summary

Reprocessed Inquiry Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
510(k) Number
K203261
510(k) Type
Special
Applicant
Innovative Health, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2021
Days to Decision
120 days
Submission Type
Summary