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Reprocessed Inquiry Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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