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PATHWAY ACCESS SHEATH CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030662
510(k) Type
Traditional
Applicant
VERTELINK CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2003
Days to Decision
184 days
Submission Type
Statement

PATHWAY ACCESS SHEATH CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030662
510(k) Type
Traditional
Applicant
VERTELINK CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2003
Days to Decision
184 days
Submission Type
Statement