K231066
- 510(k) number
- K231066
- Device name
- CuratOR EX3242-FD
- Applicant
- Eizo Corporation JP
- Product code
- GCJ — Laparoscope, General & Plastic Surgery
- Decision date
- 2023-12-18
- Date received
- 2023-04-14
- 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: K231066.pdf
Official FDA record: K231066
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.