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Gatekeeper Balloon Catheter

Page Type
Cleared 510(K)
510(k) Number
K192786
510(k) Type
Traditional
Applicant
Arch Catheter, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2020
Days to Decision
208 days
Submission Type
Summary

Gatekeeper Balloon Catheter

Page Type
Cleared 510(K)
510(k) Number
K192786
510(k) Type
Traditional
Applicant
Arch Catheter, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2020
Days to Decision
208 days
Submission Type
Summary