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