I.L. Med, Inc. · Class II · Cleared Mar 5, 1991
| K-number | K905511 |
| Device name | CODMAN NEUROLASE LASER SYSTEM/MODIFICATION |
| Applicant | I.L. Med, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Mar 5, 1991 |
| 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