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ANGIOMED RENAL DILATION SET

Page Type
Cleared 510(K)
510(k) Number
K855140
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1986
Days to Decision
60 days

ANGIOMED RENAL DILATION SET

Page Type
Cleared 510(K)
510(k) Number
K855140
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1986
Days to Decision
60 days