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Ablacon, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230008Ablamap® SystemJune 8, 2023
K223666Ablacath™ Mapping CatheterMarch 17, 2023
K203084Ablamap SoftwareAugust 31, 2021