Iridex Corp · Class II · Cleared Oct 8, 2002
| K-number | K022228 |
| Device name | FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES |
| Applicant | Iridex Corp |
| Product code | GEX |
| Device class | Class II |
| Decision date | Oct 8, 2002 |
| 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