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LANDMARK VENOUS ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K910799
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1991
Days to Decision
24 days

LANDMARK VENOUS ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K910799
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1991
Days to Decision
24 days