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091 Balloon Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K231629
510(k) Type
Special
Applicant
EOSolutions, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2023
Days to Decision
148 days
Submission Type
Summary

091 Balloon Guide Catheter

Page Type
Cleared 510(K)
510(k) Number
K231629
510(k) Type
Special
Applicant
EOSolutions, Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2023
Days to Decision
148 days
Submission Type
Summary