LYSUS INFUSION SYSTEM— 510(k) K041629

Substantially Equivalent

Ekos Corp.

FDA 510(k) clearance K041629 for LYSUS INFUSION SYSTEM, Substantially Equivalent on 2004-08-06. Applicant: Ekos Corp..

Clearance details

Applicant: Ekos Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 2004-06-16
Decision date: 2004-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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