Aaron Medical Industries · Class I · Cleared May 2, 1995
| K-number | K950520 |
| Device name | BURR, CORNEAL, BATTERY-POWERED |
| Applicant | Aaron Medical Industries |
| Product code | HOG |
| Device class | Class I |
| Decision date | May 2, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 886.4070 |
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