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MODIFICATION TO MODIFIED HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092298
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2009
Days to Decision
99 days
Submission Type
Summary

MODIFICATION TO MODIFIED HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K092298
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2009
Days to Decision
99 days
Submission Type
Summary