K223739
- 510(k) number
- K223739
- Device name
- VS Tabletop Tonometer
- Applicant
- Medimaging Integrated Solution, Inc. CN
- Product code
- HKX — Tonometer, Ac-Powered
- Decision date
- 2023-11-08
- Date received
- 2022-12-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 3.3 MB · U.S. public domain
Also available from FDA: K223739.pdf
Official FDA record: K223739
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.