Quanta Dialysis Technologies, Ltd.

FDA Regulatory Profile

Quanta Dialysis Technologies, Ltd. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 1, 2024

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K242269SC+ Hemodialysis Device (SC-14269); Dialysate Cartridge (SC-14656); Blood Tube Set (SC-14651)Nov 1, 2024
K222067SC+ Hemodialysis Device, SC+ Dialysate Cartridge, SC+ Blood Tube SetNov 10, 2022
K210661SC+ Hemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood TubesetAug 12, 2021
K193670SC+ Haemodialysis Machine, SC+ Dialysate Cartridge, SC+ Blood Tube SetDec 23, 2020