K252636
- 510(k) number
- K252636
- Device name
- Fluido Compact System
- Applicant
- The Surgical Company International B.V. NL
- Product code
- LGZ — Warmer, Thermal, Infusion Fluid
- Decision date
- 2025-11-18
- Date received
- 2025-08-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252636.pdf
Official FDA record: K252636
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.