LXN — Probe, Test, Heart-Valve Class I
FDA Device Classification
Classification Details
- Product Code
- LXN
- Device Class
- Class I
- Regulation Number
- 870.4500
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K890165 | dhason brothers | FORCEPS-ORTHOPEDIC | February 13, 1989 |
| K881449 | baxter healthcare | EDWARDS-DUROMEDICS LEAFLET PROBE, MODEL 1116 | June 15, 1988 |