DXP
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Transducer, Vessel Occlusion
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2890
- Medical specialty
- Cardiovascular
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT (K891180) | Ingress Technologies, Inc. | 1989-06-15 |
| UNICUFF (K812639) | Frontier Products | 1981-10-02 |
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Every clearance here is in the API, with alerts when new ones post.