K233516
- 510(k) number
- K233516
- Device name
- Tono-Vera® Tonometer and Ocu-Dot® Tonometer Probes (16305, 16306, 16318)
- Applicant
- Reichert, Inc. NY · US
- Product code
- HKY — Tonometer, Manual
- Decision date
- 2024-05-01
- Date received
- 2023-11-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K233516.pdf
Official FDA record: K233516
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.