Last synced on 14 November 2025 at 11:06 pm

DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT

Page Type
Cleared 510(K)
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)
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