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Telescope Guide Extension Catheter

Page Type
Cleared 510(K)
510(k) Number
K183353
510(k) Type
Traditional
Applicant
Medtronic Inc.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
109 days
Submission Type
Summary

Telescope Guide Extension Catheter

Page Type
Cleared 510(K)
510(k) Number
K183353
510(k) Type
Traditional
Applicant
Medtronic Inc.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
3/22/2019
Days to Decision
109 days
Submission Type
Summary