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ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101651
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
28 days
Submission Type
Summary

ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101651
510(k) Type
Special
Applicant
Cordis Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2010
Days to Decision
28 days
Submission Type
Summary