Last synced on 25 January 2026 at 3:41 am

AMSURE RED RUBBER URETHRAL CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030293
510(k) Type
Traditional
Applicant
Amsino International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2004
Days to Decision
372 days
Submission Type
Statement

AMSURE RED RUBBER URETHRAL CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030293
510(k) Type
Traditional
Applicant
Amsino International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2004
Days to Decision
372 days
Submission Type
Statement