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ANGIOFLOW

Page Type
Cleared 510(K)
510(k) Number
K854910
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1986
Days to Decision
220 days

ANGIOFLOW

Page Type
Cleared 510(K)
510(k) Number
K854910
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1986
Days to Decision
220 days