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Cross Vascular, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232809Cross Vascular RF Generator and Footswitch (optional accessory)October 12, 2023
K232852Cross Vascular RF Transseptal Needle, Cross Vascular Connection CableOctober 12, 2023