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PowerGlide Pro™ Midline Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240359
510(k) Type
Traditional
Applicant
Becton, Dickinson and Company (Bard Access Systems, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2024
Days to Decision
174 days
Submission Type
Summary

PowerGlide Pro™ Midline Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240359
510(k) Type
Traditional
Applicant
Becton, Dickinson and Company (Bard Access Systems, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2024
Days to Decision
174 days
Submission Type
Summary