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Reprocessed Response Diagnostic Electrophysiology Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182488
510(k) Type
Traditional
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
164 days
Submission Type
Summary

Reprocessed Response Diagnostic Electrophysiology Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182488
510(k) Type
Traditional
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/2019
Days to Decision
164 days
Submission Type
Summary