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MODIFIED HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K080583
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2008
Days to Decision
137 days
Submission Type
Summary

MODIFIED HD GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K080583
510(k) Type
Special
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2008
Days to Decision
137 days
Submission Type
Summary