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HARBOR CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K881884
510(k) Type
Traditional
Applicant
HARBOR MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
85 days

HARBOR CENTRAL VENOUS CATHETER

Page Type
Cleared 510(K)
510(k) Number
K881884
510(k) Type
Traditional
Applicant
HARBOR MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
85 days