Ekos Corp.
Ekos Corp. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2008.
Top product codes for Ekos Corp.
Recent clearances by Ekos Corp.
- K081467 — EKOSONIC ENDOVASCULAR SYSTEM WITH RAPID PULSE MODULATION
- K080392 — EndoWave Infusion System
- K073166 — ENDOWAVE INFUSION SYSTEM
- K072507 — ENDOWAVE INFUSION SYSTEM
- K071933 — ENDOWAVE INFUSION SYSTEM
- K063620 — EKOS MICRO-INFUSION SYSTEM
- K062508 — NEUROWAVE MICRO-INFUSION SYSTEM
- K062507 — MICRO-INFUSION SYSTEM
- K060422 — LYSUS INFUSION SYSTEM
- K060084 — LYSUS INFUSION SYSTEM
- K053437 — EKOS MICRO-INFUSION SYSTEM
- K053432 — EKOS MICRO-INFUSION SYSTEM
- K052071 — LYSUS INFUSION SYSTEM
- K051319 — LYSUS INFUSION SYSTEM
- K051225 — EKOS MICRO-INFUSION SYSTEM
- K041826 — EKOS ULTRASOUND INFUSION SYSTEM
- K050563 — EKOS PERIPHERAL INFUSION SYSTEM
- K050472 — LYSUS INFUSION SYSTEM
- K043269 — Lysus Infusion System
- K042456 — Lysus Infusion System
- K041629 — LYSUS INFUSION SYSTEM
- K033214 — EKOS PERIPHERAL INFUSION SYSTEM
- K030637 — EKOS PERIPHERAL INFUSION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.