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Kodiak™ Dual Port Coaxial Introducer Kit

Page Type
Cleared 510(K)
510(k) Number
K230631
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2023
Days to Decision
76 days
Submission Type
Summary

Kodiak™ Dual Port Coaxial Introducer Kit

Page Type
Cleared 510(K)
510(k) Number
K230631
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2023
Days to Decision
76 days
Submission Type
Summary