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GlidePath 13F Long-Term Hemodialysis Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211410
510(k) Type
Special
Applicant
Bard Peripheral Vascular, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/4/2021
Days to Decision
29 days
Submission Type
Summary

GlidePath 13F Long-Term Hemodialysis Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211410
510(k) Type
Special
Applicant
Bard Peripheral Vascular, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
6/4/2021
Days to Decision
29 days
Submission Type
Summary