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Xablecath, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K183357XableCath Crossing CatheterJanuary 21, 2019
K180986XableCath Support Catheter Product FamilyMay 15, 2018
K170041XableCath Support CatheterSeptember 7, 2017