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ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Page Type
Cleared 510(K)
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)
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