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DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011862
510(k) Type
Special
Applicant
Denver Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2001
Days to Decision
28 days
Submission Type
Summary

DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011862
510(k) Type
Special
Applicant
Denver Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2001
Days to Decision
28 days
Submission Type
Summary