Last synced on 6 June 2025 at 11:06 pm

FlexCath Select Steerable Shealth and Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163268
510(k) Type
Traditional
Applicant
Medtronic CryoCath LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2017
Days to Decision
73 days
Submission Type
Summary

FlexCath Select Steerable Shealth and Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163268
510(k) Type
Traditional
Applicant
Medtronic CryoCath LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2017
Days to Decision
73 days
Submission Type
Summary