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

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