Last synced on 14 November 2025 at 11:06 pm

Cross Vascular RF Generator and Footswitch (optional accessory)

Page Type
Cleared 510(K)
510(k) Number
K232809
510(k) Type
Traditional
Applicant
Cross Vascular Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2023
Days to Decision
30 days
Submission Type
Summary

Cross Vascular RF Generator and Footswitch (optional accessory)

Page Type
Cleared 510(K)
510(k) Number
K232809
510(k) Type
Traditional
Applicant
Cross Vascular Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/2023
Days to Decision
30 days
Submission Type
Summary