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EVALVE STEERABLE GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093866
510(k) Type
Special
Applicant
EVALVE INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
27 days
Submission Type
Summary

EVALVE STEERABLE GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093866
510(k) Type
Special
Applicant
EVALVE INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/2010
Days to Decision
27 days
Submission Type
Summary