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HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K090335
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2009
Days to Decision
85 days
Submission Type
Summary

HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K090335
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2009
Days to Decision
85 days
Submission Type
Summary