Last synced on 27 June 2025 at 11:06 pm

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173262
510(k) Type
Traditional
Applicant
Innovative Health, Llc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2018
Days to Decision
146 days
Submission Type
Summary

Reprocessed ViewFlex Xtra Ice Diagnostic Ultrasound Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173262
510(k) Type
Traditional
Applicant
Innovative Health, Llc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2018
Days to Decision
146 days
Submission Type
Summary