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AUGEASE VASCULAR AUGMENTATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101355
510(k) Type
Traditional
Applicant
AUGDVT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
165 days
Submission Type
Summary

AUGEASE VASCULAR AUGMENTATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101355
510(k) Type
Traditional
Applicant
AUGDVT LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
165 days
Submission Type
Summary