Argon Medical Devices, Inc. · Class II · Cleared Sep 10, 2024
| K-number | K242612 |
| Device name | Option ELITE Vena Cava Filter System (352506070E 352506100E) |
| Applicant | Argon Medical Devices, Inc. |
| Product code | DTK |
| Device class | Class II |
| Decision date | Sep 10, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 870.3375 |
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