K233142
- 510(k) number
- K233142
- Device name
- EndoSign® Cell collection device (ES-CYT-102)
- Applicant
- Cyted Limited GB
- Product code
- EOX — Esophagoscope (Flexible Or Rigid)
- Decision date
- 2024-01-19
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233142.pdf
Official FDA record: K233142
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.