Last synced on 18 April 2025 at 11:05 pm

GUIDANT RETRIEVER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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