LYSUS INFUSION SYSTEM— 510(k) K060422

Substantially Equivalent

Ekos Corp.

FDA 510(k) clearance K060422 for LYSUS INFUSION SYSTEM, Substantially Equivalent on 2006-03-09. Applicant: Ekos Corp..

Clearance details

Applicant: Ekos Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 2006-02-17
Decision date: 2006-03-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Bothell, WA, US

Download summary PDF View on FDA.gov ↗

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