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Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter

Page Type
Cleared 510(K)
510(k) Number
K183461
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/8/2019
Days to Decision
145 days
Submission Type
Summary

Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter

Page Type
Cleared 510(K)
510(k) Number
K183461
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
5/8/2019
Days to Decision
145 days
Submission Type
Summary