EKOS ULTRASOUND INFUSION SYSTEM— 510(k) K041826

Unknown

Ekos Corp.

FDA 510(k) clearance K041826 for EKOS ULTRASOUND INFUSION SYSTEM, Unknown on 2005-04-27. Applicant: Ekos Corp.. Device class: 2.

Clearance details

Applicant: Ekos Corp.
Product code: Code NUI
Device class: Class 2
Regulation: 21 CFR 870.1200
Advisory panel: Cardiovascular
Date received: 2004-07-07
Decision date: 2005-04-27
Decision: Unknown
Clearance type: Traditional
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NUI

K062508 — NEUROWAVE MICRO-INFUSION SYSTEM2006-12-05
K053437 — EKOS MICRO-INFUSION SYSTEM2006-01-06
K051225 — EKOS MICRO-INFUSION SYSTEM2005-06-10

More clearances from Ekos Corp.

K081467 — EKOSONIC ENDOVASCULAR SYSTEM WITH RAPID PULSE MODULATION2008-06-26
K080392 — EndoWave Infusion System2008-04-30
K073166 — ENDOWAVE INFUSION SYSTEM2008-04-22
K072507 — ENDOWAVE INFUSION SYSTEM2007-10-04
K071933 — ENDOWAVE INFUSION SYSTEM2007-08-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.