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ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY

Page Type
Cleared 510(K)
510(k) Number
K855142
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1986
Days to Decision
75 days

ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY

Page Type
Cleared 510(K)
510(k) Number
K855142
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1986
Days to Decision
75 days