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Hemodia Sas

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221919DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing setsMarch 9, 2023
K203480DOUBLEFLO systemApril 5, 2021
K192921Zeos Aqua Vision Pump and tubeOctober 9, 2020
K132883HEMODIA ARTHROSCOPY PUMP TUBE SETS (HATS)November 1, 2013