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Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202042
510(k) Type
Special
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
120 days
Submission Type
Summary

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202042
510(k) Type
Special
Applicant
Innovative Health, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2020
Days to Decision
120 days
Submission Type
Summary