Last synced on 25 April 2025 at 11:05 pm

Kodiak™ Dual Port Coaxial Introducer Kit

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