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PowerGlide Pro™ Midline Catheter

Page Type
Cleared 510(K)
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)
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