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AMSURE 3-WAY HYDROPHILIC LATEX FOLEY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101824
510(k) Type
Traditional
Applicant
Amsino International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2010
Days to Decision
74 days
Submission Type
Summary

AMSURE 3-WAY HYDROPHILIC LATEX FOLEY CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101824
510(k) Type
Traditional
Applicant
Amsino International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/2010
Days to Decision
74 days
Submission Type
Summary