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LIFEVALVE CENTRAL VENOUS CATHTER

Page Type
Cleared 510(K)
510(k) Number
K031718
510(k) Type
Special
Applicant
HORIZON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2003
Days to Decision
29 days
Submission Type
Summary

LIFEVALVE CENTRAL VENOUS CATHTER

Page Type
Cleared 510(K)
510(k) Number
K031718
510(k) Type
Special
Applicant
HORIZON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2003
Days to Decision
29 days
Submission Type
Summary