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VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002650
510(k) Type
Traditional
Applicant
BENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2001
Days to Decision
175 days
Submission Type
Summary

VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002650
510(k) Type
Traditional
Applicant
BENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2001
Days to Decision
175 days
Submission Type
Summary