Remington Medical, Inc. · Class II · Cleared Aug 30, 2024
| K-number | K241583 |
| Device name | VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01) |
| Applicant | Remington Medical, Inc. |
| Product code | DPW |
| Device class | Class II |
| Decision date | Aug 30, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 870.2100 |
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