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PowerGlide Pro Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K162377
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2016
Days to Decision
29 days
Submission Type
Summary

PowerGlide Pro Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K162377
510(k) Type
Special
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2016
Days to Decision
29 days
Submission Type
Summary