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ULTRA LOW POROSITY DACRON WOVEN PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921659
510(k) Type
Traditional
Applicant
INTERVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/25/1992
Days to Decision
232 days
Submission Type
Statement

ULTRA LOW POROSITY DACRON WOVEN PATCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921659
510(k) Type
Traditional
Applicant
INTERVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
11/25/1992
Days to Decision
232 days
Submission Type
Statement