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Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232130
510(k) Type
Traditional
Applicant
Surgical Instrument Services and Savings, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2023
Days to Decision
151 days
Submission Type
Summary

Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232130
510(k) Type
Traditional
Applicant
Surgical Instrument Services and Savings, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2023
Days to Decision
151 days
Submission Type
Summary