K233190
- 510(k) number
- K233190
- Device name
- ENFit Adaptor
- Applicant
- Jiangsu Caina Medical Co.,Ltd CN
- Product code
- PIO — Enteral Specific Transition Connectors
- Decision date
- 2024-01-18
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.9 MB · U.S. public domain
Also available from FDA: K233190.pdf
Official FDA record: K233190
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.