K260799
- 510(k) number
- K260799
- Device name
- Nipro Dry Acid Concentrate Mixer
- Applicant
- Nipro Technical Solutions, Incoporated AZ · US
- Product code
- KPO — Dialysate Concentrate For Hemodialysis (Liquid Or Po
- Decision date
- 2026-08-19
- Date received
- 2026-03-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K260799.pdf
Official FDA record: K260799
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.