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MODIFIED LANDMARK VENOUS ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884259
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1988
Days to Decision
28 days

MODIFIED LANDMARK VENOUS ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K884259
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1988
Days to Decision
28 days