K243361
- 510(k) number
- K243361
- Device name
- Nutrifit
- Applicant
- Vygon USA PA · US
- Product code
- FPD — Tube, Feeding
- Decision date
- 2024-12-19
- Date received
- 2024-10-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243361.pdf
Official FDA record: K243361
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.