Last synced on 21 June 2024 at 11:04 pm

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001703
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2000
Days to Decision
120 days
Submission Type
Summary

PERCLOSE VASCULAR SUTURE DELIVERY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001703
510(k) Type
Traditional
Applicant
ABBOTT VASCULAR INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2000
Days to Decision
120 days
Submission Type
Summary