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VPI URETERAL DILATATION BALLON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813278
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1981
Days to Decision
25 days

VPI URETERAL DILATATION BALLON CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813278
510(k) Type
Traditional
Applicant
VANCE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1981
Days to Decision
25 days