FDA Product Code
FDA Product Code NUI — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Cardiovascular
- 21 CFR Citation
- 870.1200
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K062508 | NEUROWAVE MICRO-INFUSION SYSTEM | Ekos Corp. | 2006-12-05 | Special | PDF ↗ |
| K053437 | EKOS MICRO-INFUSION SYSTEM | Ekos Corp. | 2006-01-06 | Special | PDF ↗ |
| K051225 | EKOS MICRO-INFUSION SYSTEM | Ekos Corp. | 2005-06-10 | Special | PDF ↗ |
| K041826 | EKOS ULTRASOUND INFUSION SYSTEM | Ekos Corp. | 2005-04-27 | Traditional | PDF ↗ |
Product code NUI · Class II · Cardiovascular. Data: openFDA.