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VAN-TEC URETERAL DILATION BALLOON CATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841940
510(k) Type
Traditional
Applicant
VAN-TEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1984
Days to Decision
84 days

VAN-TEC URETERAL DILATION BALLOON CATH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841940
510(k) Type
Traditional
Applicant
VAN-TEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1984
Days to Decision
84 days