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UROFLEX

Page Type
Cleared 510(K)
510(k) Number
K854908
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1986
Days to Decision
95 days

UROFLEX

Page Type
Cleared 510(K)
510(k) Number
K854908
510(k) Type
Traditional
Applicant
ANGIOMED U.S., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/1986
Days to Decision
95 days