K243965
- 510(k) number
- K243965
- Device name
- Origin
- Applicant
- Nerv Technology Inc. (D.B.A.) Fluidai Medical CA
- Product code
- SFO — Electrode Measurement, Drain Effluent Ph
- Decision date
- 2025-08-21
- Date received
- 2024-12-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K243965.pdf
Official FDA record: K243965
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.