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Rusch Silicone Foley Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161770
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2017
Days to Decision
311 days
Submission Type
Summary

Rusch Silicone Foley Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161770
510(k) Type
Traditional
Applicant
Teleflex Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2017
Days to Decision
311 days
Submission Type
Summary