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Rusch Intermittent Urethral Catheters

Page Type
Cleared 510(K)
510(k) Number
K222279
510(k) Type
Special
Applicant
Teleflex Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2022
Days to Decision
31 days
Submission Type
Summary

Rusch Intermittent Urethral Catheters

Page Type
Cleared 510(K)
510(k) Number
K222279
510(k) Type
Special
Applicant
Teleflex Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2022
Days to Decision
31 days
Submission Type
Summary