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GentleCath Glide Intermittent Catheter

Page Type
Cleared 510(K)
510(k) Number
K161344
510(k) Type
Traditional
Applicant
CONVATEC LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/20/2016
Days to Decision
130 days
Submission Type
Summary

GentleCath Glide Intermittent Catheter

Page Type
Cleared 510(K)
510(k) Number
K161344
510(k) Type
Traditional
Applicant
CONVATEC LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/20/2016
Days to Decision
130 days
Submission Type
Summary