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Medline Reinforced Epidural Catheter

Page Type
Cleared 510(K)
510(k) Number
K181782
510(k) Type
Traditional
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2019
Days to Decision
244 days
Submission Type
Summary

Medline Reinforced Epidural Catheter

Page Type
Cleared 510(K)
510(k) Number
K181782
510(k) Type
Traditional
Applicant
Medline Industries, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/2019
Days to Decision
244 days
Submission Type
Summary