Neitz Instruments Company, Ltd. · Class II · Cleared Sep 30, 1997
| K-number | K972440 |
| Device name | CATARACTSCREENER CT - S |
| Applicant | Neitz Instruments Company, Ltd. |
| Product code | HKI |
| Device class | Class II |
| Decision date | Sep 30, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 886.1120 |
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