LXN
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Probe, Test, Heart-Valve
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 870.4500
- Medical specialty
- Cardiovascular
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| FORCEPS-ORTHOPEDIC (K890165) | Dhason Brothers, Inc. | 1989-02-13 |
| EDWARDS-DUROMEDICS LEAFLET PROBE, MODEL 1116 (K881449) | Baxter Healthcare Corp | 1988-06-15 |
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Every clearance here is in the API, with alerts when new ones post.