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AVD INTIMAX (TM) BILIARY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910006
510(k) Type
Traditional
Applicant
APPLIED VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1991
Days to Decision
42 days

AVD INTIMAX (TM) BILIARY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910006
510(k) Type
Traditional
Applicant
APPLIED VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1991
Days to Decision
42 days