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PERCLOSE VASCULAR SUTURE DELIVERY DEVICE

Page Type
Cleared 510(K)
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)
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