Lysus Infusion System— 510(k) K043269

Substantially Equivalent

Ekos Corp.

FDA 510(k) clearance K043269 for Lysus Infusion System, Substantially Equivalent on 2004-12-22. Applicant: Ekos Corp..

Clearance details

Applicant: Ekos Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 2004-11-26
Decision date: 2004-12-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Bothell, WA, US

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