Last synced on 14 November 2025 at 11:06 pm

Artix Ballon Guiding Sheath

Page Type
Cleared 510(K)
510(k) Number
K221846
510(k) Type
Traditional
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2022
Days to Decision
17 days
Submission Type
Summary

Artix Ballon Guiding Sheath

Page Type
Cleared 510(K)
510(k) Number
K221846
510(k) Type
Traditional
Applicant
Inari Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2022
Days to Decision
17 days
Submission Type
Summary