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GUIDANT RETRIEVER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K001694
510(k) Type
Traditional
Applicant
GUIDANT CARDIAC AND VASCULAR SURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2001
Days to Decision
347 days
Submission Type
Summary

GUIDANT RETRIEVER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K001694
510(k) Type
Traditional
Applicant
GUIDANT CARDIAC AND VASCULAR SURGERY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2001
Days to Decision
347 days
Submission Type
Summary