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PowerGlide Pro Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K153280
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
203 days
Submission Type
Summary

PowerGlide Pro Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K153280
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2016
Days to Decision
203 days
Submission Type
Summary