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MODIFICATION TO MODIFIED HD GUIDE CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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