Last synced on 14 November 2025 at 11:06 pm

MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254

Page Type
Cleared 510(K)
510(k) Number
K122581
510(k) Type
Traditional
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2012
Days to Decision
90 days
Submission Type
Summary

MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254

Page Type
Cleared 510(K)
510(k) Number
K122581
510(k) Type
Traditional
Applicant
CONCENTRIC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2012
Days to Decision
90 days
Submission Type
Summary