Last synced on 14 November 2025 at 11:06 pm

HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131

Page Type
Cleared 510(K)
510(k) Number
K091703
510(k) Type
Traditional
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
126 days
Submission Type
Summary

HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131

Page Type
Cleared 510(K)
510(k) Number
K091703
510(k) Type
Traditional
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2009
Days to Decision
126 days
Submission Type
Summary