K233126
- 510(k) number
- K233126
- Device name
- aetherSlide
- Applicant
- Aetherai Co., Ltd. TW
- Product code
- QKQ — Digital Pathology Image Viewing And Management Softw
- Decision date
- 2024-05-30
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233126.pdf
Official FDA record: K233126
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.