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..

Clearance details

Applicant: Ekos Corp.
Product code: Code NUI
Advisory panel: Cardiovascular
Date received: 2004-07-07
Decision date: 2005-04-27
Decision: Unknown
Clearance type: Traditional
Location: Bothell, WA, US

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