Last synced on 25 January 2026 at 3:41 am

Reprocessed Inquiry Optima Plus Steerable Diagnostic EP Catheter, Reprocessed Inquiry Optima Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160421
510(k) Type
Traditional
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
260 days
Submission Type
Summary

Reprocessed Inquiry Optima Plus Steerable Diagnostic EP Catheter, Reprocessed Inquiry Optima Steerable Diagnostic EP Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160421
510(k) Type
Traditional
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2016
Days to Decision
260 days
Submission Type
Summary