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ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K062531
510(k) Type
Traditional
Applicant
CORDIS CORP., A JOHNSON & JOHNSON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2006
Days to Decision
24 days
Submission Type
Summary

ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K062531
510(k) Type
Traditional
Applicant
CORDIS CORP., A JOHNSON & JOHNSON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/2006
Days to Decision
24 days
Submission Type
Summary