Reichert, Inc. · Class II · Cleared May 1, 2024
| K-number | K233516 |
| Device name | Tono-Vera® Tonometer and Ocu-Dot® Tonometer Probes (16305, 16306, 16318) |
| Applicant | Reichert, Inc. |
| Product code | HKY |
| Device class | Class II |
| Decision date | May 1, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 886.1930 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov