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LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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