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VAN-TEC FASCIAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820865
510(k) Type
Traditional
Applicant
VAN-TEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1982
Days to Decision
37 days

VAN-TEC FASCIAL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820865
510(k) Type
Traditional
Applicant
VAN-TEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1982
Days to Decision
37 days