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Hemodia Sas

FDA Regulatory Profile

Hemodia Sas has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Mar 9, 2023

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K221919DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing setsMar 9, 2023
K203480DOUBLEFLO systemApr 5, 2021
K192921Zeos Aqua Vision Pump and tubeOct 9, 2020
K132883HEMODIA ARTHROSCOPY PUMP TUBE SETS (HATS)Nov 1, 2013

FDA data resources