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LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K010767
510(k) Type
Special
Applicant
HORIZON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2001
Days to Decision
27 days
Submission Type
Summary

LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES

Page Type
Cleared 510(K)
510(k) Number
K010767
510(k) Type
Special
Applicant
HORIZON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2001
Days to Decision
27 days
Submission Type
Summary