Living Technology, Inc. · Class II · Cleared Aug 10, 1989
| K-number | K893956 |
| Device name | EAGLE LASER, SURGICAL, NEODYMIUM DOPED YTTRIUM |
| Applicant | Living Technology, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Aug 10, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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